Canonical Allele Identifier: PA2825666835
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2237240
ClinVar RCV Id: RCV002723872
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Lys77Gln
CA362007998
NM_001128209.2:c.229A>C