ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825666854
Gene: SGCD
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2448149
ClinVar RCV Id:
RCV003168198
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001121681.1:p.Lys91Glu
CA362008095
NM_001128209.2:c.271A>G