Canonical Allele Identifier: PA2826566372
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 230269
ClinVar RCV Id: RCV000217404 RCV000235558 RCV000529612 RCV003929915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Gly335Arg
CA000677
NM_001276760.3:c.1003G>C