Canonical Allele Identifier: PA1139754256
Gene: LOXHD1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653213.6:p.Asn725Ser
CA299797758
NM_144612.7:c.2174A>G