Allele Registry

Canonical Allele Identifier: PA2827651921

Gene: HLCS HGNC NCBI

ClinVar Allele:

980040

ClinVar RCV:

RCV001277488

ClinVar Variation:

989621

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339443.1:p.Tyr246Cys	CA10020706 NM_001352514.2:c.737A>G