Allele Registry

Canonical Allele Identifier: PA2741859891

Gene: NRG1 HGNC NCBI

ClinVar RCV:

RCV003982045

ClinVar Variation:

3060016

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309136.1:p.Met349Thr	CA4705942 NM_001322207.2:c.1046T>C