Canonical Allele Identifier: PA2828042895
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gly1641Asp
CA16032918
NM_001354904.2:c.4922G>A