Canonical Allele Identifier: PA1139710030
Gene: NPPA HGNC NCBI

Linked Data

ClinVar Variation Id: 857219
ClinVar RCV Id: RCV001062850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006163.1:p.Phe40Leu
CA338451670
NM_006172.4:c.120C>G
CA338451676
NM_006172.4:c.120C>A
CA338451686
NM_006172.4:c.118T>C