ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916078825
Gene: NF2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
457898
ClinVar RCV Id:
RCV000553100
RCV002286750
RCV002395308
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_861970.1:p.Ala464Val
CA030005
NM_181832.3:c.1391C>T