Canonical Allele Identifier: PA1139754161
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 891861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653213.6:p.Phe599Leu
CA8952760
NM_144612.7:c.1795T>C
CA402378882
NM_144612.7:c.1797T>A
CA402378883
NM_144612.7:c.1797T>G