Allele Registry

Canonical Allele Identifier: PA2827653465

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001991

ClinVar Variation:

1914

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339446.1:p.Leu216Arg	CA278025 NM_001352517.1:c.647T>G