Canonical Allele Identifier: PA2826558378
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1965210
ClinVar RCV Id: RCV002726636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Ser29Arg
CA382617217
NM_001276504.2:c.85A>C
CA382617223
NM_001276504.2:c.87C>A
CA382617224
NM_001276504.2:c.87C>G