Allele Registry

Canonical Allele Identifier: PA2825935979

Gene: NRG1 HGNC NCBI

ClinVar RCV:

RCV003982045

ClinVar Variation:

3060016

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153471.1:p.Met273Thr	CA4705942 NM_001159999.3:c.818T>C