Canonical Allele Identifier: PA2827980535
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_001341828.1:p.Gln2472His
CA16037641
NM_001354899.2:c.7416G>C
CA16037642
NM_001354899.2:c.7416G>T