Canonical Allele Identifier: PA658810404
Gene: NMNAT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 520701
ClinVar RCV Id: RCV004025263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055854.1:p.Arg232Gln
CA1283363
NM_015039.4:c.695G>A