Canonical Allele Identifier: PA161029
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 134883
ClinVar RCV Id: RCV000121630 RCV000220588 RCV000234708 RCV000712402 RCV002483222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035957.1:p.Cys632Ser
CA161025
NM_001042492.3:c.1894T>A
CA399005205
NM_001042492.3:c.1895G>C