Allele Registry

Canonical Allele Identifier: PA2827653102

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV001057509

ClinVar Variation:

852810

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339445.1:p.Gly494Val	CA409921894 NM_001352516.2:c.1481G>T