Canonical Allele Identifier: PA2826558113
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 465242
ClinVar RCV Id: RCV001853704 RCV003139772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Gly16Cys
CA382616751
NM_001276503.2:c.46G>T