Canonical Allele Identifier: PA1139698635
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 949408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ala80Gly
CA397844357
NM_001276761.3:c.239C>G