Allele Registry

Canonical Allele Identifier: PA2827653678

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001986

ClinVar Variation:

1909

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339446.1:p.Arg508Trp	CA278020 NM_001352517.1:c.1522C>T