Canonical Allele Identifier: PA2828031901
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220329

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala214Pro
CA047113
NM_001354904.2:c.640G>C