Canonical Allele Identifier: PA2828007447
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp1538Val
CA16032466
NM_001354905.2:c.4613A>T