Canonical Allele Identifier: PA2828018872
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Met731Val
CA16027984
NM_001354906.2:c.2191A>G