Canonical Allele Identifier: PA916035429
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 374458
ClinVar RCV Id: RCV000415893 RCV002521466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339447.1:p.Lys30Glu
CA10020742
NM_001352518.2:c.88A>G