Canonical Allele Identifier: PA645502980
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 239454
ClinVar RCV Id: RCV000233939 RCV001762528 RCV002256146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.Arg11His
CA047588
NM_003001.5:c.32G>A