Allele Registry

Canonical Allele Identifier: PA915972502

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000667229

ClinVar Variation:

552036

HGVS (amino-acid)	Matching Registered Transcripts
NP_004534.3:p.Val1491Leu	CA348815435 NM_004543.5:c.4471G>T CA348815436 NM_004543.5:c.4471G>C