Canonical Allele Identifier: PA916028650
Gene: NNT HGNC NCBI

Linked Data

ClinVar Variation Id: 35542
ClinVar RCV Id: RCV000029197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317955.1:p.Asn878Lys
CA213050
NM_001331026.2:c.2634T>G
CA359654998
NM_001331026.2:c.2634T>A