Canonical Allele Identifier: PA1139754256
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 889357
ClinVar RCV Id: RCV001123226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653213.6:p.Asn725Ser
CA299797758
NM_144612.7:c.2174A>G