Canonical Allele Identifier: PA916030368
Gene: SDCCAG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 167664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337177.1:p.Glu502Gly
CA234901
NM_001350248.2:c.1505A>G