Canonical Allele Identifier: PA2828963982
Gene: LOXHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2558611
ClinVar RCV Id: RCV003300352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371403.1:p.Arg554Trp
CA299800866
NM_001384474.1:c.1660C>T