Canonical Allele Identifier: PA2826567385
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Glu219Gly
CA16615703
NM_001276761.3:c.656A>G