ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826558102
Gene: SDHD
HGNC
NCBI
Linked Data
ClinVar Variation Id:
533789
ClinVar RCV Id:
RCV002233051
RCV002358819
RCV004003916
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263432.1:p.Ala13Ser
CA228550401
NM_001276503.2:c.37G>T