Canonical Allele Identifier: PA2826847578
Gene: NMNAT1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284708.1:p.Val9Met
CA260600
NM_001297779.2:c.25G>A