Canonical Allele Identifier: PA192718
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_002993.1:p.His102Asn
CA016659
NM_003002.4:c.304C>A