Canonical Allele Identifier: PA2573205103
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1398771
ClinVar RCV Id: RCV001922648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339443.1:p.Ile264Val
CA409913237
NM_001352514.2:c.790A>G