Canonical Allele Identifier: PA2830401989
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 527699
ClinVar RCV Id: RCV001011649 RCV000632644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861969.1:p.Met401Val
CA411149540
NM_181831.3:c.1201A>G