Canonical Allele Identifier: PA2828002897
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly1676Asp
CA16032918
NM_001354902.2:c.5027G>A