Canonical Allele Identifier: PA2826562605
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_001263626.1:p.His138Gln
CA397836436
NM_001276697.3:c.414C>G
CA397836439
NM_001276697.3:c.414C>A