Canonical Allele Identifier: PA2825164001
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2420338
ClinVar RCV Id: RCV003118863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000402.3:p.Pro53Leu
CA409913817
NM_000411.8:c.158C>T