Canonical Allele Identifier: PA2830399671
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1020490
ClinVar RCV Id: RCV001320074 RCV002402892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861968.1:p.Lys442Asn
CA411149985
NM_181830.3:c.1326A>C
CA411149986
NM_181830.3:c.1326A>T