Canonical Allele Identifier: PA2828022137
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 940870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn1248Ser
CA16031388
NM_001354906.2:c.3743A>G