Canonical Allele Identifier: PA165917
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 68308
ClinVar RCV Id: RCV000059160 RCV000130191 RCV000206280 RCV000506837 RCV001009575 RCV001535533 RCV003162463 RCV004549489
ClinVar Variation Id: 1410579
ClinVar RCV Id: RCV001928103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000258.1:p.Gly629Arg
CA165914
NM_000267.3:c.1885G>A
CA399005175
NM_000267.3:c.1885G>C