Allele Registry

Canonical Allele Identifier: PA916035396

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000492067

RCV002527063

ClinVar Variation:

428585

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.Ser662Asn	CA10020389 NM_001352514.2:c.1985G>A