Canonical Allele Identifier: PA2826304658
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2420338
ClinVar RCV Id: RCV003118863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229714.1:p.Pro53Leu
CA409913817
NM_001242785.2:c.158C>T