Canonical Allele Identifier: PA2827971038
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1320471
ClinVar RCV Id: RCV001776450
ClinVar Variation Id: 2573820
ClinVar RCV Id: RCV003318156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln2378His
CA16037029
NM_001354898.2:c.7134G>C
CA16037030
NM_001354898.2:c.7134G>T