Canonical Allele Identifier: PA2830401211
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 412217
ClinVar RCV Id: RCV001009688 RCV000477644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861969.1:p.Ala257Ser
CA16616604
NM_181831.3:c.769G>T