Canonical Allele Identifier: PA2829970001
Gene: NPAS3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3201528
ClinVar RCV Id: RCV004490873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071406.1:p.Ser607Phe
CA389413088
NM_022123.2:c.1820C>T