Canonical Allele Identifier: PA2828011920
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1351612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2358Gly
CA16037326
NM_001354902.2:c.7072A>G