Canonical Allele Identifier: PA196697
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 187084
ClinVar RCV Id: RCV000166772 RCV000478217 RCV000641906 RCV001523820 RCV004019988 RCV003995530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.His127Arg
CA011435
NM_003001.5:c.380A>G