Canonical Allele Identifier: PA2826566471
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 481098
ClinVar RCV Id: RCV000571144 RCV003621549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Phe15Leu
CA397846420
NM_001276761.3:c.45C>G
CA397846422
NM_001276761.3:c.45C>A
CA397846436
NM_001276761.3:c.43T>C