ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825666912
Gene: SGCD
HGNC
NCBI
Linked Data
ClinVar Variation Id:
411706
ClinVar RCV Id:
RCV000458794
RCV000596325
RCV002339185
RCV002489082
RCV003233644
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001121681.1:p.Asp152Gly
CA3530601
NM_001128209.2:c.455A>G