Canonical Allele Identifier: PA2828007467
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Met923Val
CA16027984
NM_001354902.2:c.2767A>G