Allele Registry

Canonical Allele Identifier: PA915972418

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000153548

RCV001272991

RCV001542997

ClinVar Variation:

167336

HGVS (amino-acid)	Matching Registered Transcripts
NP_004534.3:p.Tyr1301His	CA180211 NM_004543.5:c.3901T>C