Canonical Allele Identifier: PA2826561716
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Ser264Gly
CA000491
NM_001276696.3:c.790A>G