Canonical Allele Identifier: PA2580183945
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 2118541
ClinVar RCV Id: RCV003030531 RCV004009278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Gly64Arg
CA382617418
NM_001276504.2:c.190G>C