Canonical Allele Identifier: PA2825643786
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2300Gly
CA046510
NM_001127511.3:c.6898A>G