Canonical Allele Identifier: PA2827652289
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1389284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339444.1:p.Asn156Ile
CA320395694
NM_001352515.2:c.467A>T