Canonical Allele Identifier: PA2830394866
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072476
ClinVar RCV Id: RCV004013498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861966.1:p.Phe467Leu
CA411149702
NM_181828.3:c.1399T>C
CA411149708
NM_181828.3:c.1401C>A
CA411149709
NM_181828.3:c.1401C>G