Allele Registry

Canonical Allele Identifier: PA916035370

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001991

ClinVar Variation:

1914

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.Leu363Arg	CA278025 NM_001352514.2:c.1088T>G