Canonical Allele Identifier: PA105158
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000402.3:p.Asp571Asn
CA278019
NM_000411.8:c.1711G>A