Canonical Allele Identifier: PA2828028086
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg2156His
CA16037262
NM_001354906.2:c.6467G>A