Allele Registry

Canonical Allele Identifier: PA915972500

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000081137

RCV000348796

RCV000589707

RCV001542995

ClinVar Variation:

95131

HGVS (amino-acid)	Matching Registered Transcripts
NP_004534.3:p.Val1491Met	CA148238 NM_004543.5:c.4471G>A