Canonical Allele Identifier: PA916078863
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_861970.1:p.Glu545Asp
CA411150123
NM_181832.3:c.1635A>C
CA411150124
NM_181832.3:c.1635A>T