Canonical Allele Identifier: PA645510843
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 438435
ClinVar RCV Id: RCV000505381 RCV001857228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Leu80Arg
CA382617293
NM_003002.4:c.239T>G