Canonical Allele Identifier: PA645510725
Gene: NMNAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 438133
ClinVar RCV Id: RCV000504848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073624.2:p.Ser162Tyr
CA338686519
NM_022787.4:c.485C>A