Canonical Allele Identifier: PA916006133
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 185719
ClinVar RCV Id: RCV000165195 RCV002228740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.His63Asn
CA016659
NM_001276504.2:c.187C>A