Canonical Allele Identifier: PA2828007507
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly1543Arg
CA16032494
NM_001354905.2:c.4627G>A
CA16032495
NM_001354905.2:c.4627G>C