Canonical Allele Identifier: PA2826558585
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 156154
ClinVar RCV Id: RCV000144172 RCV000454533 RCV000505355 RCV001023072 RCV000994727 RCV002228513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Leu120_Ter121insLeuProPhe
CA016726
NM_001276504.2:c.362G>T