Canonical Allele Identifier: PA2825135661
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 662489
ClinVar RCV Id: RCV000820145 RCV001759604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Met519Ile
CA411149776
NM_000268.4:c.1557G>T
CA411149777
NM_000268.4:c.1557G>A
CA411149778
NM_000268.4:c.1557G>C