Canonical Allele Identifier: PA2829833631
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072476
ClinVar RCV Id: RCV004013498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057502.2:p.Phe509Leu
CA411149702
NM_016418.5:c.1525T>C
CA411149708
NM_016418.5:c.1527C>A
CA411149709
NM_016418.5:c.1527C>G