Canonical Allele Identifier: PA2826558079
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 581402
ClinVar RCV Id: RCV002534431 RCV003999764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Arg6Ser
CA382616662
NM_001276503.2:c.18G>C
CA382616664
NM_001276503.2:c.18G>T