Canonical Allele Identifier: PA260601
Gene: NMNAT1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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