Canonical Allele Identifier: PA2827652545
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2142709
ClinVar RCV Id: RCV003076376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339444.1:p.Ala499Thr
CA10020423
NM_001352515.2:c.1495G>A