Canonical Allele Identifier: PA2828964202
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 889357
ClinVar RCV Id: RCV001123226
JSON-LD

Amino-acid Alleles

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