Canonical Allele Identifier: PA2828016434
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 572572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn344Ser
CA16025430
NM_001354906.2:c.1031A>G