ClinGen Allele Registry
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Canonical Allele Identifier:
PA645502086
Gene: LOXHD1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000219519
RCV000485022
RCV001126895
RCV002271468
ClinVar Variation:
228819
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_653213.6:p.Arg899Pro
CA8952632
NM_144612.7:c.2696G>C