Allele Registry

Canonical Allele Identifier: PA148228

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000081132

RCV000398581

RCV000587497

RCV001542973

ClinVar Variation:

95126

HGVS (amino-acid)	Matching Registered Transcripts
NP_004534.2:p.Ile6546Val	CA148226 NM_004543.4:c.19636A>G CA891842684 NM_004543.4:c.19635_19636delinsTG