Allele Registry

Canonical Allele Identifier: PA2827651851

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000487407

RCV001139291

ClinVar Variation:

418248

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.Glu149Lys	CA16620992 NM_001352514.2:c.445G>A