Canonical Allele Identifier: PA2573303633
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1388716
ClinVar RCV Id: RCV001878027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653213.6:p.Thr596Arg
CA402378902
NM_144612.7:c.1787C>G