Canonical Allele Identifier: PA1139734646
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 895131
ClinVar RCV Id: RCV001137043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Glu71Lys
CA409913579
NM_001352518.2:c.211G>A