Allele Registry

Canonical Allele Identifier: PA260601

Gene: NMNAT1 HGNC NCBI

ClinVar RCV:

RCV000030771

ClinVar Variation:

37140

HGVS (amino-acid)	Matching Registered Transcripts
NP_073624.2:p.Val9Met	CA260600 NM_022787.4:c.25G>A