Allele Registry

Canonical Allele Identifier: PA916035390

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000799673

ClinVar Variation:

645566

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.Met640Val	CA10020428 NM_001352514.2:c.1918A>G