Canonical Allele Identifier: PA107819
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 6897
ClinVar RCV Id: RCV000007305 RCV000020520 RCV000567104 RCV001701480 RCV002288471 RCV002512869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Asp92Tyr
CA016702
NM_003002.4:c.274G>T