Canonical Allele Identifier: PA093278
Gene: NMNAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 37134
ClinVar RCV Id: RCV000030765 RCV000255806 RCV001003567 RCV000504859 RCV001075816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284707.1:p.Glu257Lys
CA342906
NM_001297778.1:c.769G>A