Allele Registry

Canonical Allele Identifier: PA2826304613

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000487407

RCV001139291

ClinVar Variation:

418248

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229714.1:p.Glu2Lys	CA16620992 NM_001242785.2:c.4G>A