Canonical Allele Identifier: PA260591
Gene: NMNAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 37133
ClinVar RCV Id: RCV000030764 RCV001090803
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073624.2:p.Arg207Trp
CA260590
NM_022787.4:c.619C>T