Canonical Allele Identifier: PA2826567278
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376580
ClinVar RCV Id: RCV000420256 RCV000421654 RCV000420917 RCV000422298 RCV000431682 RCV000430938 RCV000432990 RCV000432344 RCV000438862 RCV000442778 RCV000441640 RCV003621530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Cys203Trp
CA16603005
NM_001276761.3:c.609C>G