Allele Registry

Canonical Allele Identifier: PA2829746608

Gene: NRG1 HGNC NCBI

ClinVar RCV:

RCV003982045

ClinVar Variation:

3060016

HGVS (amino-acid)	Matching Registered Transcripts
NP_039254.1:p.Met289Thr	CA4705942 NM_013960.5:c.866T>C