Canonical Allele Identifier: PA2826564869
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 230112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Ala30Gly
CA10580956
NM_001276760.3:c.89C>G