Canonical Allele Identifier: PA1139698628
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 837018
ClinVar RCV Id: RCV001038262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Gly78Val
CA397844396
NM_001276761.3:c.233G>T