Canonical Allele Identifier: PA916006199
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 465238
ClinVar RCV Id: RCV002526127 RCV003999154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Gly99Val
CA382619290
NM_001276504.2:c.296G>T