Canonical Allele Identifier: PA2827502774
Gene: SDCCAG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 260015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337176.1:p.Val21Ile
CA1483504
NM_001350247.2:c.61G>A