Canonical Allele Identifier: PA215738
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 41670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000258.1:p.Thr862Ser
CA215735
NM_000267.3:c.2585C>G
CA398984375
NM_000267.3:c.2584A>T