Canonical Allele Identifier: PA2828964050
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3119591
ClinVar RCV Id: RCV004410414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371403.1:p.Asn603Ser
CA402378858
NM_001384474.1:c.1808A>G