Allele Registry

Canonical Allele Identifier: PA915972461

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000247985

RCV000514092

RCV001084411

ClinVar Variation:

257814

HGVS (amino-acid)	Matching Registered Transcripts
NP_004534.3:p.Asn1402Lys	CA1910700 NM_004543.5:c.4206T>A CA348816568 NM_004543.5:c.4206T>G