Canonical Allele Identifier: PA916078832
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 527690
ClinVar RCV Id: RCV000632635 RCV002388018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861970.1:p.Pro482Leu
CA031430
NM_181832.3:c.1445C>T