Canonical Allele Identifier: PA2828964022
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 891862
ClinVar RCV Id: RCV001127409 RCV002558257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371403.1:p.Thr584Met
CA8952763
NM_001384474.1:c.1751C>T