Allele Registry

Canonical Allele Identifier: PA2826305037

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001987

ClinVar Variation:

1910

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229714.1:p.Gly581Ser	CA278021 NM_001242785.2:c.1741G>A