Canonical Allele Identifier: PA2829866192
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2713613
ClinVar RCV Id: RCV003501347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057502.2:p.Phe307Leu
CA411145695
NM_016418.5:c.919T>C
CA411145712
NM_016418.5:c.921T>A
CA411145714
NM_016418.5:c.921T>G