Canonical Allele Identifier: PA2830394169
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 457930
ClinVar RCV Id: RCV000533798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861966.1:p.His262Arg
CA411145642
NM_181828.3:c.785A>G