Canonical Allele Identifier: PA2826558345
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 2935574
ClinVar RCV Id: RCV003793668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Gly19Asp
CA382617156
NM_001276504.2:c.56G>A