Allele Registry

Canonical Allele Identifier: PA2827653485

Gene: HLCS HGNC NCBI

ClinVar RCV:

RCV000001984

ClinVar Variation:

1907

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339446.1:p.Leu237Pro	CA278018 NM_001352517.1:c.710T>C