Canonical Allele Identifier: PA2828030682
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn2709Ser
CA015484
NM_001354903.2:c.8126A>G