Canonical Allele Identifier: PA291181
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 137550
ClinVar RCV Id: RCV000125362 RCV000337767 RCV001572921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000402.3:p.Val96Ile
CA291180
NM_000411.8:c.286G>A