Canonical Allele Identifier: PA2826558528
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412502
ClinVar RCV Id: RCV002230660 RCV002356711 RCV004002009 RCV003476142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Ala94Asp
CA071351
NM_001276504.2:c.281C>A