Canonical Allele Identifier: PA2828964005
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1393104
ClinVar RCV Id: RCV001896561
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371403.1:p.Asn572Lys
CA402379057
NM_001384474.1:c.1716C>A
CA402379058
NM_001384474.1:c.1716C>G