Canonical Allele Identifier: PA2830394177
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2713613
ClinVar RCV Id: RCV003501347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861966.1:p.Phe265Leu
CA411145695
NM_181828.3:c.793T>C
CA411145712
NM_181828.3:c.795T>A
CA411145714
NM_181828.3:c.795T>G