Canonical Allele Identifier: PA2828029620
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg2387Gly
CA16038727
NM_001354906.2:c.7159A>G