Canonical Allele Identifier: PA2826558651
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 947980
ClinVar RCV Id: RCV001819909 RCV002241392 RCV002339577 RCV003129736 RCV004010724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Arg17Gly
CA382616758
NM_001276506.2:c.49C>G