Canonical Allele Identifier: PA2830398172
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 426373
ClinVar RCV Id: RCV000489141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861968.1:p.Phe79Leu
CA411142186
NM_181830.3:c.235T>C
CA411142191
NM_181830.3:c.237T>A
CA411142192
NM_181830.3:c.237T>G