Allele Registry

Canonical Allele Identifier: PA645439116

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV000337361

ClinVar Variation:

285736

HGVS (amino-acid)	Matching Registered Transcripts
NP_000014.1:p.Thr208Ile	CA10605223 NM_000023.3:c.623C>T