Canonical Allele Identifier: PA2826847579
Gene: NMNAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 195375
ClinVar RCV Id: RCV000175940 RCV001074101 RCV001256640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284708.1:p.Ala13Thr
CA241796
NM_001297779.2:c.37G>A