Allele Registry

Canonical Allele Identifier: PA2827653687

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000492067

RCV002527063

ClinVar Variation:

428585

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339446.1:p.Ser515Asn	CA10020389 NM_001352517.1:c.1544G>A