Canonical Allele Identifier: PA2828007890
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 423629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly1607Asp
CA16032918
NM_001354905.2:c.4820G>A