Canonical Allele Identifier: PA142188
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 47919
ClinVar RCV Id: RCV000041191 RCV000887253 RCV001123332
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653213.6:p.Asp570Asn
CA142187
NM_144612.7:c.1708G>A