Allele Registry

Canonical Allele Identifier: PA2826304237

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000815726

ClinVar Variation:

658832

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229713.1:p.Leu237Arg	CA409912461 NM_001242784.3:c.710T>G