Canonical Allele Identifier: PA2828028640
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_001341832.1:p.Gln2399His
CA16037641
NM_001354903.2:c.7197G>C
CA16037642
NM_001354903.2:c.7197G>T