Canonical Allele Identifier: PA2825378173
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 1414418
ClinVar RCV Id: RCV001930460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030590.1:p.Trp76Arg
CA343456702
NM_001035513.2:c.226T>A
CA343456704
NM_001035513.2:c.226T>C