Canonical Allele Identifier: PA2825666794
Gene: SGCD HGNC NCBI
ClinVar RCV:
RCV000172778
ClinVar Variation:
192194
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Arg30Gly
CA200046
NM_001128209.2:c.88C>G