Canonical Allele Identifier: PA2829865938
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2914086
ClinVar RCV Id: RCV003607119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057502.2:p.His158Tyr
CA411142162
NM_016418.5:c.472C>T