Allele Registry

Canonical Allele Identifier: PA658673356

Gene: SDHC HGNC NCBI

ClinVar Variation Id: 465977

HGVS (amino-acid)	Matching Registered Transcripts
NP_002992.1:p.Ala2Thr	CA343354908 NM_003001.5:c.4G>A