Canonical Allele Identifier: PA2825377536
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 1718074
ClinVar RCV Id: RCV002296534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030588.1:p.Tyr59Asp
CA343361362
NM_001035511.2:c.175T>G