Allele Registry

Canonical Allele Identifier: PA2827653662

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000799673

ClinVar Variation:

645566

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339446.1:p.Met493Val	CA10020428 NM_001352517.1:c.1477A>G