Allele Registry

Canonical Allele Identifier: PA105259

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001991

ClinVar Variation:

1914

HGVS (amino-acid)	Matching Registered Transcripts
NP_000402.3:p.Leu216Arg	CA278025 NM_000411.8:c.647T>G