Allele Registry

Canonical Allele Identifier: PA916035399

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001988

RCV000185961

ClinVar Variation:

1911

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.Val697Met	CA278022 NM_001352514.2:c.2089G>A