Allele Registry

Canonical Allele Identifier: PA2827652931

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000408618

ClinVar Variation:

369667

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339445.1:p.Gly241Ala	CA10654770 NM_001352516.2:c.722G>C