Canonical Allele Identifier: PA1139746277
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 547704
ClinVar RCV Id: RCV000660131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861966.1:p.Phe77del
CA645600895
NM_181828.3:c.231_233del