Allele Registry

Canonical Allele Identifier: PA2829545408

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000081132

RCV000398581

RCV000587497

RCV000693166

RCV001542973

RCV002499240

ClinVar Variation:

95126

571908

HGVS (amino-acid)	Matching Registered Transcripts
NP_004534.3:p.Ile6546Val	CA148226 NM_004543.5:c.19636A>G CA891842684 NM_004543.5:c.19635_19636delinsTG