Allele Registry

Canonical Allele Identifier: PA105266

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001984

ClinVar Variation:

1907

HGVS (amino-acid)	Matching Registered Transcripts
NP_000402.3:p.Leu237Pro	CA278018 NM_000411.8:c.710T>C