ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2830391695
Gene: NF2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2434338
ClinVar RCV Id:
RCV003131795
RCV004246030
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_861546.1:p.Pro135Ser
CA411153803
NM_181825.3:c.403C>T