Canonical Allele Identifier: PA2827654022
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 898132
ClinVar RCV Id: RCV001141810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Thr251Ala
CA409912382
NM_001352518.2:c.751A>G