Canonical Allele Identifier: PA2828026562
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2084Asn
CA045325
NM_001354903.2:c.6251G>A