Canonical Allele Identifier: PA2830399532
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3231080
ClinVar RCV Id: RCV004523194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861968.1:p.Pro413Ala
CA411149616
NM_181830.3:c.1237C>G