Canonical Allele Identifier: PA107876
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 6900
ClinVar RCV Id: RCV000007309 RCV000155750 RCV000221353 RCV002228004 RCV001810833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Tyr114Cys
CA016797
NM_003002.4:c.341A>G