Allele Registry

Canonical Allele Identifier: PA2825981452

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000153548

RCV001272991

RCV001542997

ClinVar Variation:

167336

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157979.2:p.Tyr1301His	CA180211 NM_001164507.2:c.3901T>C