Canonical Allele Identifier: PA2573247812
Gene: NPPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1437686
ClinVar RCV Id: RCV001934072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006163.1:p.Phe17Leu
CA597126
NM_006172.4:c.49T>C
CA338451965
NM_006172.4:c.51C>G
CA338451967
NM_006172.4:c.51C>A