Canonical Allele Identifier: PA2826304721
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1389284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229714.1:p.Asn156Ile
CA320395694
NM_001242785.2:c.467A>T