Canonical Allele Identifier: PA161069
Gene: NF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 41673
ClinVar RCV Id: RCV000034585 RCV000121638 RCV000129680 RCV000199175 RCV000264802 RCV000268253 RCV000323382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035957.1:p.Asp176Glu
CA161065
NM_001042492.3:c.528T>A
CA398985091
NM_001042492.3:c.528T>G