Canonical Allele Identifier: PA1139741872
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 946681
ClinVar RCV Id: RCV003538615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His2609Arg
CA16038215
NM_001354896.2:c.7826A>G