Allele Registry

Canonical Allele Identifier: PA645379481

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000408618

ClinVar Variation:

369667

HGVS (amino-acid)	Matching Registered Transcripts
NP_000402.3:p.Gly241Ala	CA10654770 NM_000411.8:c.722G>C