Allele Registry

Canonical Allele Identifier: PA916035416

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000224257

ClinVar Variation:

235250

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.His816Tyr	CA10581253 NM_001352514.2:c.2446C>T