Canonical Allele Identifier: PA118552
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 6895
ClinVar RCV Id: RCV000007300 RCV000007302 RCV000007299 RCV000034697 RCV000122006 RCV000162470 RCV000988742 RCV002228001 RCV001807000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Gly12Ser
CA016980
NM_003002.4:c.34G>A