ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826558631
Gene: SDHD
HGNC
NCBI
Linked Data
ClinVar Variation Id:
465235
ClinVar RCV Id:
RCV003476278
RCV002528396
RCV004023999
RCV003900170
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263435.1:p.Gly12Asp
CA071285
NM_001276506.2:c.35G>A