ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA211887
Gene: SGCD
HGNC
NCBI
Linked Data
ClinVar Variation Id:
161391
ClinVar RCV Id:
RCV000148887
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000328.2:p.Gly76Cys
CA211885
NM_000337.6:c.226G>T