Canonical Allele Identifier: PA2825135773
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 457904
ClinVar RCV Id: RCV000557509 RCV001012778 RCV000765631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Asp567Glu
CA10175568
NM_000268.4:c.1701C>G
CA411150407
NM_000268.4:c.1701C>A