Canonical Allele Identifier: PA2827653911
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2202147
ClinVar RCV Id: RCV002664013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Ala123Val
CA10020697
NM_001352518.2:c.368C>T