Canonical Allele Identifier: PA1139733826
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 899243
ClinVar RCV Id: RCV001143616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339443.1:p.Tyr314Cys
CA10020672
NM_001352514.2:c.941A>G