Allele Registry

Canonical Allele Identifier: PA2825936009

Gene: NRG1 HGNC NCBI

ClinVar RCV:

RCV003982045

ClinVar Variation:

3060016

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153473.1:p.Met239Thr	CA4705942 NM_001160001.3:c.716T>C