Allele Registry

Canonical Allele Identifier: PA2825994069

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000081132

RCV000398581

RCV000587497

RCV000693166

RCV001542973

RCV002499240

ClinVar Variation:

95126

571908

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157980.2:p.Ile8402Val	CA148226 NM_001164508.2:c.25204A>G CA891842684 NM_001164508.2:c.25203_25204delinsTG