Canonical Allele Identifier: PA2828003679
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Glu2117Ala
CA045546
NM_001354902.2:c.6350A>C