Canonical Allele Identifier: PA2826558534
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1060148
ClinVar RCV Id: RCV002242642 RCV002329384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Cys101Tyr
CA382619315
NM_001276504.2:c.302G>A