Allele Registry

Canonical Allele Identifier: PA915977600

Gene: SGCA HGNC NCBI

ClinVar RCV:

RCV000178022

RCV000344242

ClinVar Variation:

197094

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129169.1:p.Ala107Val	CA245046 NM_001135697.3:c.320C>T