Canonical Allele Identifier: PA2825135712
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2842037
ClinVar RCV Id: RCV003608189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000259.1:p.Glu541Asp
CA411150099
NM_000268.4:c.1623A>C
CA411150100
NM_000268.4:c.1623A>T