Canonical Allele Identifier: PA2826558536
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 578342
ClinVar RCV Id: RCV000764955 RCV002233358 RCV000986023 RCV003165869 RCV003999713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Tyr102His
CA382619325
NM_001276504.2:c.304T>C