Canonical Allele Identifier: PA916035372
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 658832
ClinVar RCV Id: RCV000815726

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339443.1:p.Leu384Arg
CA409912461
NM_001352514.2:c.1151T>G