Allele Registry

Canonical Allele Identifier: PA2826534606

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000667229

ClinVar Variation:

552036

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258137.2:p.Val1491Leu	CA348815435 NM_001271208.2:c.4471G>T CA348815436 NM_001271208.2:c.4471G>C