Allele Registry

Canonical Allele Identifier: PA3057316451

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV004800118

ClinVar Variation:

3384982

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129169.1:p.Arg98Ser	CA400177900 NM_001135697.3:c.292C>A