Canonical Allele Identifier: PA2827652321
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2201826
ClinVar RCV Id: RCV002644526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339444.1:p.Asp188Asn
CA10020655
NM_001352515.2:c.562G>A