Canonical Allele Identifier: PA2826566757
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12370
ClinVar RCV Id: RCV000013169 RCV000079203 RCV000219702 RCV000421928 RCV000422996 RCV000426058 RCV000427411 RCV000431507 RCV000440887 RCV000438074 RCV000443020 RCV000429847 RCV000420199 RCV000420869 RCV000435681 RCV000424996 RCV000432585 RCV000433689 RCV000440140 RCV000443379 RCV000633355 RCV000785532 RCV001257523 RCV002288487
ClinVar Variation Id: 2700111
ClinVar RCV Id: RCV003510506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro112Ser
CA000200
NM_001276761.3:c.334C>T
CA2697552104
NM_001276761.3:c.334_335delinsAG