Canonical Allele Identifier: PA1139746917
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 963971
ClinVar RCV Id: RCV001238097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861970.1:p.Lys515Arg
CA411149749
NM_181832.3:c.1544A>G