Canonical Allele Identifier: PA2827996030
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp1639Gly
CA16032465
NM_001354901.2:c.4916A>G