Canonical Allele Identifier: PA2827966438
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1063950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ala986Val
CA16027966
NM_001354898.2:c.2957C>T