Allele Registry

Canonical Allele Identifier: PA2829746528

Gene: NRG1 HGNC NCBI

ClinVar RCV:

RCV003982045

ClinVar Variation:

3060016

HGVS (amino-acid)	Matching Registered Transcripts
NP_039251.2:p.Met286Thr	CA4705942 NM_013957.5:c.857T>C