Canonical Allele Identifier: PA2826919084
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 891649
ClinVar RCV Id: RCV001127075 RCV002556772 RCV003246710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294942.1:p.Glu346Lys
CA8952316
NM_001308013.2:c.1036G>A