Canonical Allele Identifier: PA2826847600
Gene: NMNAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 438132
ClinVar RCV Id: RCV000504653 RCV001314168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284708.1:p.Gly52Val
CA579169
NM_001297779.2:c.155G>T