Allele Registry

Canonical Allele Identifier: PA916035372

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000815726

ClinVar Variation:

658832

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.Leu384Arg	CA409912461 NM_001352514.2:c.1151T>G