Canonical Allele Identifier: PA2830399691
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2135982
ClinVar RCV Id: RCV003059830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861968.1:p.Lys448Asn
CA411150029
NM_181830.3:c.1344G>C
CA411150030
NM_181830.3:c.1344G>T