Canonical Allele Identifier: PA2830285328
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3119610
ClinVar RCV Id: RCV004410433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653213.6:p.Lys1544Glu
CA402373360
NM_144612.7:c.4630A>G