Allele Registry

Canonical Allele Identifier: PA2826304993

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV003468353

ClinVar Variation:

2676026

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229714.1:p.Asn511Lys	CA409921204 NM_001242785.2:c.1533T>A CA409921207 NM_001242785.2:c.1533T>G