Allele Registry

Canonical Allele Identifier: PA915972076

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000641321

RCV003148813

RCV003472031

RCV003488752

ClinVar Variation:

533979

HGVS (amino-acid)	Matching Registered Transcripts
NP_004534.3:p.Asp498Gly	CA348825220 NM_004543.5:c.1493A>G