Canonical Allele Identifier: PA2828023636
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gly1484Asp
CA16032918
NM_001354906.2:c.4451G>A