Allele Registry

Canonical Allele Identifier: PA2827151089

Gene: NRG1 HGNC NCBI

ClinVar RCV:

RCV003982045

ClinVar Variation:

3060016

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309126.1:p.Met132Thr	CA4705942 NM_001322197.2:c.395T>C