Allele Registry

Canonical Allele Identifier: PA196697

Gene: SDHC HGNC NCBI

ClinVar Allele:

181599

ClinVar RCV:

RCV000166772

RCV000478217

RCV000641906

RCV001523820

RCV003995530

RCV004019988

ClinVar Variation:

187084

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