Canonical Allele Identifier: PA2827652227
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 203759
ClinVar RCV Id: RCV000185950 RCV002513956 RCV004020253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339444.1:p.Glu54Gln
CA312603
NM_001352515.2:c.160G>C