Canonical Allele Identifier: PA916006112
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 486441
ClinVar RCV Id: RCV000573596 RCV002232173 RCV004001130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Met70Ile
CA228555656
NM_001276503.2:c.210G>A
CA382618939
NM_001276503.2:c.210G>C
CA382618942
NM_001276503.2:c.210G>T