Canonical Allele Identifier: PA2827989436
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1351612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2408Gly
CA16037326
NM_001354900.2:c.7222A>G