Canonical Allele Identifier: PA2826566084
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 660046
ClinVar RCV Id: RCV000817167
ClinVar Variation Id: 926470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.His258Gln
CA397836436
NM_001276760.3:c.774C>G
CA397836439
NM_001276760.3:c.774C>A