Canonical Allele Identifier: PA2828011446
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2227Gly
CA046510
NM_001354902.2:c.6679A>G