Canonical Allele Identifier: PA2828965418
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2060362
ClinVar RCV Id: RCV002938767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371403.1:p.Asn1552Ser
CA402373299
NM_001384474.1:c.4655A>G