Canonical Allele Identifier: PA2827996051
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gly1644Arg
CA16032494
NM_001354901.2:c.4930G>A
CA16032495
NM_001354901.2:c.4930G>C