Allele Registry

Canonical Allele Identifier: PA091234

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV000077936

RCV000169164

ClinVar Variation:

92301

HGVS (amino-acid)	Matching Registered Transcripts
NP_000014.1:p.Arg34His	CA199071 NM_000023.3:c.101G>A