Canonical Allele Identifier: PA2829970000
Gene: NPAS3 HGNC NCBI

Linked Data

ClinVar Variation Id: 718529
ClinVar RCV Id: RCV000891497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071406.1:p.Ser587Arg
CA7150898
NM_022123.2:c.1761C>G
CA389412835
NM_022123.2:c.1759A>C
CA389412845
NM_022123.2:c.1761C>A