Allele Registry

Canonical Allele Identifier: PA915972300

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000081134

RCV000265121

RCV000589189

RCV001543000

ClinVar Variation:

95128

HGVS (amino-acid)	Matching Registered Transcripts
NP_004534.3:p.Lys1027Asn	CA148230 NM_004543.5:c.3081A>T CA348820602 NM_004543.5:c.3081A>C