Allele Registry

Canonical Allele Identifier: PA2825935936

Gene: NRG1 HGNC NCBI

ClinVar RCV:

RCV003982045

ClinVar Variation:

3060016

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153467.1:p.Met256Thr	CA4705942 NM_001159995.3:c.767T>C