Canonical Allele Identifier: PA2828011603
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2261Gly
CA16036702
NM_001354902.2:c.6781A>G