Allele Registry

Canonical Allele Identifier: PA260591

Gene: NMNAT1 HGNC NCBI

ClinVar RCV:

RCV000030764

RCV001090803

ClinVar Variation:

37133

HGVS (amino-acid)	Matching Registered Transcripts
NP_073624.2:p.Arg207Trp	CA260590 NM_022787.4:c.619C>T