Canonical Allele Identifier: PA2826919074
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2059368
ClinVar RCV Id: RCV002933695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294942.1:p.Ala331Thr
CA8952319
NM_001308013.2:c.991G>A