Canonical Allele Identifier: PA2826558388
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 486442
ClinVar RCV Id: RCV000575825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Val33del
CA658658103
NM_001276504.2:c.96_98del