Canonical Allele Identifier: PA2828001404
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1009641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp931Gly
CA16028046
NM_001354902.2:c.2792A>G