Canonical Allele Identifier: PA2825135477
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1522072
ClinVar RCV Id: RCV002046454 RCV002372820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Met426Leu
CA411148411
NM_000268.4:c.1276A>C
CA411148413
NM_000268.4:c.1276A>T