Canonical Allele Identifier: PA1139731592
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 957959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Met2731Val
CA16039002
NM_001354896.2:c.8191A>G