Allele Registry

Canonical Allele Identifier: PA1139734052

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV001057509

ClinVar Variation:

852810

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.Gly641Val	CA409921894 NM_001352514.2:c.1922G>T