Canonical Allele Identifier: PA2826304831
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 203763
ClinVar RCV Id: RCV000185954 RCV000814306 RCV004020254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229714.1:p.Val284Ile
CA312611
NM_001242785.2:c.850G>A