Canonical Allele Identifier: PA2830391829
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 689695
ClinVar RCV Id: RCV000850449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861546.1:p.Met179Val
CA411142552
NM_181825.3:c.535A>G