Canonical Allele Identifier: PA193497
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 185958
ClinVar Variation Id: 457763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000258.1:p.Glu1908Asp
CA193494
NM_000267.3:c.5724G>C
CA399010474
NM_000267.3:c.5724G>T