Canonical Allele Identifier: PA2826558408
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 438435
ClinVar RCV Id: RCV000505381 RCV001857228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Leu41Arg
CA382617293
NM_001276504.2:c.122T>G