Canonical Allele Identifier: PA2825666804
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2178479
ClinVar RCV Id: RCV002595557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Phe37Leu
CA130594220
NM_001128209.2:c.109T>C
CA362007720
NM_001128209.2:c.111T>G
CA362007721
NM_001128209.2:c.111T>A