Canonical Allele Identifier: PA2825164187
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 658832
ClinVar RCV Id: RCV000815726

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000402.3:p.Leu237Arg
CA409912461
NM_000411.8:c.710T>G