Allele Registry

Canonical Allele Identifier: PA2825936052

Gene: NRG1 HGNC NCBI

ClinVar RCV:

RCV003982045

ClinVar Variation:

3060016

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153476.1:p.Met286Thr	CA4705942 NM_001160004.3:c.857T>C