Canonical Allele Identifier: PA2827652806
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1123231
ClinVar RCV Id: RCV001454173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339445.1:p.Asp88Asn
CA10020712
NM_001352516.2:c.262G>A