Canonical Allele Identifier: PA2826847512
Gene: NMNAT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 438133
ClinVar RCV Id: RCV000504848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284707.1:p.Ser162Tyr
CA338686519
NM_001297778.1:c.485C>A