Canonical Allele Identifier: PA645502133
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_653213.6:p.Gly1615Arg
CA8952288
NM_144612.7:c.4843G>C
CA8952289
NM_144612.7:c.4843G>A