ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA891852289
Gene: NF2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
578288
ClinVar RCV Id:
RCV001026080
RCV002305530
RCV000701250
RCV003460968
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_057502.2:p.Ala238Val
CA323111825
NM_016418.5:c.713C>T