Allele Registry

Canonical Allele Identifier: PA2825988657

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000688136

RCV002487463

RCV003133235

ClinVar Variation:

331509

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157980.2:p.Pro1556Ser	CA1910565 NM_001164508.2:c.4666C>T