Canonical Allele Identifier: PA2825616168
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_001119589.1:p.His165Gln
CA397836436
NM_001126117.1:c.495C>G
CA397836439
NM_001126117.1:c.495C>A