Canonical Allele Identifier: PA2828002077
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala1267Val
CA008903
NM_001354902.2:c.3800C>T