Allele Registry

Canonical Allele Identifier: PA915972529

Gene: NEB HGNC NCBI

ClinVar Allele:

284721

ClinVar RCV:

RCV000688136

RCV002487463

RCV003133235

ClinVar Variation:

331509

HGVS (amino-acid)	Matching Registered Transcripts
NP_004534.3:p.Pro1556Ser	CA1910565 NM_004543.5:c.4666C>T