Canonical Allele Identifier: PA2826558460
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 21351
ClinVar RCV Id: RCV000020521 RCV001701640 RCV002433463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Leu56Pro
CA016647
NM_001276504.2:c.167T>C