ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916078784
Gene: NF2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
412217
ClinVar RCV Id:
RCV001009688
RCV000477644
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_861970.1:p.Ala340Ser
CA16616604
NM_181832.3:c.1018G>T