Canonical Allele Identifier: PA916006183
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 662467
ClinVar RCV Id: RCV002345889 RCV002235395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Lys86Arg
CA382619046
NM_001276504.2:c.257A>G