Canonical Allele Identifier: PA2827991390
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His191Arg
CA16022971
NM_001354901.2:c.572A>G