Canonical Allele Identifier: PA2827654010
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 658832
ClinVar RCV Id: RCV000815726

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Leu237Arg
CA409912461
NM_001352518.2:c.710T>G