Canonical Allele Identifier: PA2827999386
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 957959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Met2654Val
CA16039002
NM_001354901.2:c.7960A>G