Canonical Allele Identifier: PA2828028503
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759217
ClinVar Variation Id: 1759218
ClinVar RCV Id: RCV002391624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gln2217His
CA16037641
NM_001354906.2:c.6651G>C
CA16037642
NM_001354906.2:c.6651G>T