Canonical Allele Identifier: PA916041500
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg2543His
CA013862
NM_001354896.2:c.7628G>A