Canonical Allele Identifier: PA2827653908
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1398771
ClinVar RCV Id: RCV001922648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Ile117Val
CA409913237
NM_001352518.2:c.349A>G