Canonical Allele Identifier: PA2826220402
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 30036
ClinVar RCV Id: RCV000022936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184148.1:p.Phe104Ser
CA128848
NM_001197219.2:c.311T>C