Canonical Allele Identifier: PA916042617
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ile881Val
CA16028993
NM_001354906.2:c.2641A>G