ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826558509
Gene: SDHD
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1734455
ClinVar RCV Id:
RCV002349225
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263433.1:p.Lys86Glu
CA382619040
NM_001276504.2:c.256A>G