Canonical Allele Identifier: PA645502054
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 326868
ClinVar RCV Id: RCV000382843 RCV002521161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653213.6:p.Val573Ile
CA8952765
NM_144612.7:c.1717G>A