Canonical Allele Identifier: PA2826847457
Gene: NMNAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 190977
ClinVar RCV Id: RCV000171148 RCV001075815 RCV001256641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284707.1:p.Asn18Ser
CA235735
NM_001297778.1:c.53A>G