Canonical Allele Identifier: PA2830397256
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1770382
ClinVar RCV Id: RCV002387730 RCV003464510 RCV003774273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861967.1:p.Arg406Ser
CA411148809
NM_181829.3:c.1218G>C
CA411148810
NM_181829.3:c.1218G>T