Canonical Allele Identifier: PA2827502602
Gene: SDCCAG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 167664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337175.1:p.Glu169Gly
CA234901
NM_001350246.2:c.506A>G