Allele Registry

Canonical Allele Identifier: PA916035393

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001986

ClinVar Variation:

1909

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.Arg655Trp	CA278020 NM_001352514.2:c.1963C>T