Allele Registry

Canonical Allele Identifier: PA103769

Gene: HYLS1 HGNC NCBI

ClinVar RCV:

RCV000001202

RCV000454127

RCV000802696

ClinVar Variation:

1143

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128265.1:p.Asp211Gly	CA114795 NM_001134793.2:c.632A>G