Allele Registry

Canonical Allele Identifier: PA2825936063

Gene: NRG1 HGNC NCBI

ClinVar RCV:

RCV003974300

ClinVar Variation:

3059329

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153477.1:p.Arg38Gln	CA4705476 NM_001160005.2:c.113G>A