Allele Registry

Canonical Allele Identifier: PA2826535075

Gene: NEB HGNC NCBI

ClinVar Variation Id: 465620

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258137.2:p.Leu1980Ser	CA1910237 NM_001271208.2:c.5939T>C