Canonical Allele Identifier: PA2825378185
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 1737359
ClinVar RCV Id: RCV002321278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030590.1:p.Leu82Ser
CA343456775
NM_001035513.2:c.245T>C