Canonical Allele Identifier: PA2826558372
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1399449
ClinVar RCV Id: RCV001917685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Thr28Ala
CA382617211
NM_001276504.2:c.82A>G
CA658658102
NM_001276504.2:c.82_84delinsGCC