Allele Registry

Canonical Allele Identifier: PA2827652546

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV002900317

ClinVar Variation:

2044654

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339444.1:p.Ala499Val	CA10020421 NM_001352515.2:c.1496C>T