Canonical Allele Identifier: PA2826558850
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 640638
ClinVar RCV Id: RCV002535895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Cys88Phe
CA382617337
NM_001276506.2:c.263G>T