Canonical Allele Identifier: PA2828028642
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg2242His
CA013862
NM_001354906.2:c.6725G>A