Allele Registry

Canonical Allele Identifier: PA916003972

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000589010

RCV000601389

ClinVar Variation:

496132

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258137.2:p.Ser6366Ile	CA1907773 NM_001271208.2:c.19097G>T