Allele Registry

Canonical Allele Identifier: PA105145

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001986

ClinVar Variation:

1909

HGVS (amino-acid)	Matching Registered Transcripts
NP_000402.3:p.Arg508Trp	CA278020 NM_000411.8:c.1522C>T