Canonical Allele Identifier: PA2828963989
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1521433
ClinVar RCV Id: RCV002046301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371403.1:p.Gly562Arg
CA402379124
NM_001384474.1:c.1684G>C