ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2573305620
Gene: SGCD
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1465719
ClinVar RCV Id:
RCV001963789
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_758447.1:p.Gly81Ala
CA362008023
NM_172244.3:c.242G>C