Canonical Allele Identifier: PA2826558563
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1923369
ClinVar RCV Id: RCV002634571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Cys111Ser
CA228555748
NM_001276504.2:c.331T>A
CA382619480
NM_001276504.2:c.332G>C