Allele Registry

Canonical Allele Identifier: PA658677795

Gene: NEXMIF HGNC NCBI

ClinVar RCV:

RCV000712140

RCV002497186

RCV004024269

ClinVar Variation:

474071

HGVS (amino-acid)	Matching Registered Transcripts
NP_001008537.1:p.Met1237Leu	CA10454917 NM_001008537.3:c.3709A>T CA413664922 NM_001008537.3:c.3709A>C