Canonical Allele Identifier: PA2826919134
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 402259
ClinVar RCV Id: RCV000454364 RCV004022537
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294942.1:p.Gly408Arg
CA8952288
NM_001308013.2:c.1222G>C
CA8952289
NM_001308013.2:c.1222G>A