Canonical Allele Identifier: PA2826304137
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1398771
ClinVar RCV Id: RCV001922648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229713.1:p.Ile117Val
CA409913237
NM_001242784.3:c.349A>G