Canonical Allele Identifier: PA2826558258
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1733584
ClinVar RCV Id: RCV002452475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Arg73Ser
CA382618992
NM_001276503.2:c.219A>C
CA382618993
NM_001276503.2:c.219A>T