Canonical Allele Identifier: PA2827652828
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2202147
ClinVar RCV Id: RCV002664013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339445.1:p.Ala123Val
CA10020697
NM_001352516.2:c.368C>T