Canonical Allele Identifier: PA2828003257
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His1874Arg
CA16034228
NM_001354902.2:c.5621A>G