Allele Registry

Canonical Allele Identifier: PA915973173

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000117776

RCV000383498

RCV000587395

RCV001054369

RCV001543083

ClinVar Variation:

129761

850241

HGVS (amino-acid)	Matching Registered Transcripts
NP_004534.3:p.Ser2912Pro	CA154047 NM_004543.5:c.8734T>C CA916080281 NM_004543.5:c.8733_8734delinsAC