Canonical Allele Identifier: PA2827948549
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asn2810Ser
CA015484
NM_001354895.2:c.8429A>G