Canonical Allele Identifier: PA645386829
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 435976
ClinVar RCV Id: RCV000499490 RCV000703302 RCV002404314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057502.2:p.Glu545Asp
CA411150123
NM_016418.5:c.1635A>C
CA411150124
NM_016418.5:c.1635A>T