Canonical Allele Identifier: PA1139739624
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly1721Arg
CA16032494
NM_001354896.2:c.5161G>A
CA16032495
NM_001354896.2:c.5161G>C