Canonical Allele Identifier: PA2827992086
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Met407Val
CA027319
NM_001354901.2:c.1219A>G