Allele Registry

Canonical Allele Identifier: PA2829543192

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000589010

RCV000601389

ClinVar Variation:

496132

HGVS (amino-acid)	Matching Registered Transcripts
NP_004534.3:p.Ser4665Ile	CA1907773 NM_004543.5:c.13994G>T