Allele Registry

Canonical Allele Identifier: PA2741895716

Gene: MSN HGNC NCBI

ClinVar RCV:

RCV003335985

RCV003661046

ClinVar Variation:

2584545

HGVS (amino-acid)	Matching Registered Transcripts
NP_002435.1:p.Arg293Cys	CA413412704 NM_002444.3:c.877C>T