Allele Registry

Canonical Allele Identifier: PA2825935966

Gene: NRG1 HGNC NCBI

ClinVar RCV:

RCV003974300

ClinVar Variation:

3059329

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153471.1:p.Arg17Gln	CA4705476 NM_001159999.3:c.50G>A