Allele Registry

Canonical Allele Identifier: PA2826304562

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000224257

ClinVar Variation:

235250

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229713.1:p.His669Tyr	CA10581253 NM_001242784.3:c.2005C>T