Allele Registry

Canonical Allele Identifier: PA2830398791

Gene: NF2 HGNC NCBI

ClinVar Variation Id: 2713613

HGVS (amino-acid)	Matching Registered Transcripts
NP_861968.1:p.Phe224Leu	CA411145695 NM_181830.3:c.670T>C CA411145712 NM_181830.3:c.672T>A CA411145714 NM_181830.3:c.672T>G