Allele Registry

Canonical Allele Identifier: PA105343

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001988

RCV000185961

ClinVar Variation:

1911

HGVS (amino-acid)	Matching Registered Transcripts
NP_000402.3:p.Val550Met	CA278022 NM_000411.8:c.1648G>A