ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828964419
Gene: LOXHD1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000607679
RCV001275060
RCV002531137
ClinVar Variation:
505028
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001371403.1:p.Arg899Gln
CA299794546
NM_001384474.1:c.2696G>A