Canonical Allele Identifier: PA194665
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn2792Ser
CA015484
NM_001127511.3:c.8375A>G