Canonical Allele Identifier: PA2827652925
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 1430113
ClinVar RCV Id: RCV001931338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339445.1:p.Leu237Ile
CA409912463
NM_001352516.2:c.709C>A