Allele Registry

Canonical Allele Identifier: PA260597

Gene: NMNAT1 HGNC NCBI

ClinVar RCV:

RCV000030769

ClinVar Variation:

37138

HGVS (amino-acid)	Matching Registered Transcripts
NP_073624.2:p.Arg237Leu	CA260596 NM_022787.4:c.710G>T