ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA341951
Gene: SDHD
HGNC
NCBI
Linked Data
ClinVar Variation Id:
21351
ClinVar RCV Id:
RCV000020521
RCV001701640
RCV002433463
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002993.1:p.Leu95Pro
CA016647
NM_003002.4:c.284T>C