Canonical Allele Identifier: PA2826560685
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1732774
ClinVar RCV Id: RCV002454984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Ala80Asp
CA397844368
NM_001276696.3:c.239C>A