ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA891852335
Gene: NF2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
567951
ClinVar RCV Id:
RCV000688163
RCV001011729
RCV002284426
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_057502.2:p.Pro490Leu
CA031751
NM_016418.5:c.1469C>T