Canonical Allele Identifier: PA2827652384
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1399075
ClinVar RCV Id: RCV001922722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339444.1:p.Thr266Pro
CA10020615
NM_001352515.2:c.796A>C