Canonical Allele Identifier: PA2499297599
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1199288
ClinVar RCV Id: RCV001563774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653213.6:p.His556Asp
CA402379164
NM_144612.7:c.1666C>G