Canonical Allele Identifier: PA2828963998
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 47919
ClinVar RCV Id: RCV000041191 RCV000887253 RCV001123332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371403.1:p.Asp570Asn
CA142187
NM_001384474.1:c.1708G>A