Allele Registry

Canonical Allele Identifier: PA2828964202

Gene: LOXHD1 HGNC NCBI

ClinVar RCV:

RCV001123226

ClinVar Variation:

889357

HGVS (amino-acid)	Matching Registered Transcripts
NP_001371403.1:p.Asn725Ser	CA299797758 NM_001384474.1:c.2174A>G