Canonical Allele Identifier: PA2826847606
Gene: NMNAT1 HGNC NCBI
ClinVar RCV:
RCV001344745
ClinVar Variation:
1041004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284708.1:p.Pro62Thr
CA579176
NM_001297779.2:c.184C>A