Canonical Allele Identifier: PA2828011124
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2158Gly
CA046510
NM_001354905.2:c.6472A>G