Allele Registry

Canonical Allele Identifier: PA260599

Gene: NMNAT1 HGNC NCBI

ClinVar RCV:

RCV000030770

ClinVar Variation:

37139

HGVS (amino-acid)	Matching Registered Transcripts
NP_073624.2:p.Leu153Val	CA260598 NM_022787.4:c.457C>G