Canonical Allele Identifier: PA2827651902
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 895131
ClinVar RCV Id: RCV001137043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339443.1:p.Glu218Lys
CA409913579
NM_001352514.2:c.652G>A