Canonical Allele Identifier: PA2827949795
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 818459
ClinVar RCV Id: RCV001010061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His388Arg
CA16023850
NM_001354896.2:c.1163A>G