Canonical Allele Identifier: PA2826304141
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2202147
ClinVar RCV Id: RCV002664013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229713.1:p.Ala123Val
CA10020697
NM_001242784.3:c.368C>T