Allele Registry

Canonical Allele Identifier: PA2825982104

Gene: NEB HGNC NCBI

ClinVar Variation Id: 465620

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157979.2:p.Leu1980Ser	CA1910237 NM_001164507.2:c.5939T>C