Allele Registry

Canonical Allele Identifier: PA2825935956

Gene: NRG1 HGNC NCBI

ClinVar RCV:

RCV003982045

ClinVar Variation:

3060016

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153468.1:p.Met135Thr	CA4705942 NM_001159996.3:c.404T>C