Allele Registry

Canonical Allele Identifier: PA916035374

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000408618

ClinVar Variation:

369667

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.Gly388Ala	CA10654770 NM_001352514.2:c.1163G>C