Canonical Allele Identifier: PA2826558276
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 2673996
ClinVar RCV Id: RCV003450597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Gln84Glu
CA382619191
NM_001276503.2:c.250C>G