ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2830394226
Gene: NF2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
41681
ClinVar RCV Id:
RCV000034593
RCV000632655
RCV002381286
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_861966.1:p.Glu286Val
CA021461
NM_181828.3:c.857A>T