Canonical Allele Identifier: PA2829637078
Gene: PDE4D HGNC NCBI
ClinVar RCV:
RCV000033154
ClinVar Variation:
40064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006194.2:p.Ala168Val
CA130730
NM_006203.5:c.503C>T