Canonical Allele Identifier: PA2830399719
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1470191
ClinVar RCV Id: RCV001964063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861968.1:p.Glu454Ala
CA411150068
NM_181830.3:c.1361A>C