Canonical Allele Identifier: PA2826561717
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 230695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Ser264Asn
CA10580912
NM_001276696.3:c.791G>A