Canonical Allele Identifier: PA2741927047
Gene: NPPA HGNC NCBI

Linked Data

ClinVar Variation Id: 3004476
ClinVar RCV Id: RCV003866115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006163.1:p.Ala16Val
CA597127
NM_006172.4:c.47C>T