Allele Registry

Canonical Allele Identifier: PA105236

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001987

ClinVar Variation:

1910

HGVS (amino-acid)	Matching Registered Transcripts
NP_000402.3:p.Gly581Ser	CA278021 NM_000411.8:c.1741G>A