Canonical Allele Identifier: PA2827652405
Gene: HLCS HGNC NCBI

Linked Data

ClinVar Variation Id: 2461885
ClinVar RCV Id: RCV003184950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339444.1:p.Gly294Asp
CA10020597
NM_001352515.2:c.881G>A