Allele Registry

Canonical Allele Identifier: PA2827653832

Gene: HLCS HGNC NCBI

ClinVar Allele:

1128798

ClinVar RCV:

RCV001452857

ClinVar Variation:

1122278

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339446.1:p.Asp691Asn	CA10020231 NM_001352517.1:c.2071G>A