Allele Registry

Canonical Allele Identifier: PA2826304972

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000799673

ClinVar Variation:

645566

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229714.1:p.Met493Val	CA10020428 NM_001242785.2:c.1477A>G