Canonical Allele Identifier: PA161018
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 134881
ClinVar RCV Id: RCV000121628 RCV000129662 RCV000200171 RCV000587577 RCV001124835 RCV001124837 RCV001124836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000258.1:p.Ser665Phe
CA161015
NM_000267.3:c.1994C>T