Canonical Allele Identifier: PA645510735
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 438444
ClinVar RCV Id: RCV000505336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.Gly73Asp
CA343365949
NM_003001.5:c.218G>A