Allele Registry

Canonical Allele Identifier: PA2826304997

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000492067

RCV002527063

ClinVar Variation:

428585

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229714.1:p.Ser515Asn	CA10020389 NM_001242785.2:c.1544G>A