Allele Registry

Canonical Allele Identifier: PA2827151705

Gene: NRG1 HGNC NCBI

ClinVar RCV:

RCV003982045

ClinVar Variation:

3060016

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309135.1:p.Met349Thr	CA4705942 NM_001322206.2:c.1046T>C