Canonical Allele Identifier: PA658665912
Gene: NMNAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 464670
ClinVar RCV Id: RCV000538650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073624.2:p.Leu239Ser
CA579318
NM_022787.4:c.716T>C