Allele Registry

Canonical Allele Identifier: PA2573205112

Gene: HLCS HGNC NCBI

ClinVar Variation Id: 1430113

ClinVar RCV Id: RCV001931338

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.Leu384Ile	CA409912463 NM_001352514.2:c.1150C>A