ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2830397615
Gene: NF2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1431398
ClinVar RCV Id:
RCV001972057
RCV002397942
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_861967.1:p.His493Arg
CA411150049
NM_181829.3:c.1478A>G