Canonical Allele Identifier: PA2827652241
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1139368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339444.1:p.Ser83Asn
CA10020717
NM_001352515.2:c.248G>A