Canonical Allele Identifier: PA2826558097
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 465235
ClinVar RCV Id: RCV003476278 RCV002528396 RCV004023999 RCV003900170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Gly12Asp
CA071285
NM_001276503.2:c.35G>A