Canonical Allele Identifier: PA2828023558
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly1620Asp
CA10578397
NM_001354903.2:c.4859G>A