Canonical Allele Identifier: PA916078683
Gene: NF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 412211
ClinVar RCV Id: RCV000472642 RCV001020352 RCV003463971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_861966.1:p.Gln73His
CA030265
NM_181828.3:c.219A>T
CA411153358
NM_181828.3:c.219A>C