Allele Registry

Canonical Allele Identifier: PA2826304419

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV003076376

ClinVar Variation:

2142709

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229713.1:p.Ala499Thr	CA10020423 NM_001242784.3:c.1495G>A