Canonical Allele Identifier: PA2827654000
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2202514
ClinVar RCV Id: RCV002630000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Asp228His
CA409912528
NM_001352518.2:c.682G>C