Canonical Allele Identifier: PA2828005382
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 818937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Val351Asp
CA16024206
NM_001354902.2:c.1052T>A