Allele Registry

Canonical Allele Identifier: PA2741864122

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV003468353

ClinVar Variation:

2676026

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.Asn658Lys	CA409921204 NM_001352514.2:c.1974T>A CA409921207 NM_001352514.2:c.1974T>G