Allele Registry

Canonical Allele Identifier: PA2825981695

Gene: NEB HGNC NCBI

ClinVar Allele:

284721

ClinVar RCV:

RCV000688136

RCV002487463

RCV003133235

ClinVar Variation:

331509

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157979.2:p.Pro1556Ser	CA1910565 NM_001164507.2:c.4666C>T