Allele Registry

Canonical Allele Identifier: PA2827652904

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001991

ClinVar Variation:

1914

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339445.1:p.Leu216Arg	CA278025 NM_001352516.2:c.647T>G