Canonical Allele Identifier: PA166292
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141747
ClinVar RCV Id: RCV000130378 RCV000680625 RCV000206873 RCV002453461 RCV000764108 RCV003330502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000258.1:p.Ala1202Ser
CA166289
NM_000267.3:c.3604G>T