Allele Registry

Canonical Allele Identifier: PA2580208628

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV003076376

ClinVar Variation:

2142709

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.Ala646Thr	CA10020423 NM_001352514.2:c.1936G>A