Allele Registry

Canonical Allele Identifier: PA2826304217

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001991

ClinVar Variation:

1914

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229713.1:p.Leu216Arg	CA278025 NM_001242784.3:c.647T>G