Canonical Allele Identifier: PA2826220698
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 40064
ClinVar RCV Id: RCV000033154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184150.1:p.Ala2Val
CA130730
NM_001197221.2:c.5C>T