Canonical Allele Identifier: PA2825135002
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2818038
ClinVar RCV Id: RCV003607926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Met179Ile
CA411142557
NM_000268.4:c.537G>T
CA411142558
NM_000268.4:c.537G>C
CA411142559
NM_000268.4:c.537G>A