Canonical Allele Identifier: PA2828013120
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2706Gly
CA015444
NM_001354902.2:c.8116A>G