Canonical Allele Identifier: PA2826220219
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 30037
ClinVar RCV Id: RCV000022937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184147.1:p.Ser126Ala
CA128850
NM_001197218.2:c.376T>G