Canonical Allele Identifier: PA235736
Gene: NMNAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073624.2:p.Asn18Ser
CA235735
NM_022787.4:c.53A>G