Canonical Allele Identifier: PA2826006195
Gene: NPAS3 HGNC NCBI

Linked Data

ClinVar Variation Id: 718529
ClinVar RCV Id: RCV000891497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159365.1:p.Ser589Arg
CA7150898
NM_001165893.2:c.1767C>G
CA389412835
NM_001165893.2:c.1765A>C
CA389412845
NM_001165893.2:c.1767C>A