Canonical Allele Identifier: PA916006202
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 187700
ClinVar RCV Id: RCV000167450 RCV000478572 RCV002228995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Gly99Arg
CA017004
NM_001276504.2:c.295G>A
CA382619281
NM_001276504.2:c.295G>C