Canonical Allele Identifier: PA2825598847
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1347666
ClinVar RCV Id: RCV002041814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Asp61Val
CA397846191
NM_001126112.3:c.182A>T