Canonical Allele Identifier: PA2826304101
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 203759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229713.1:p.Glu54Gln
CA312603
NM_001242784.3:c.160G>C