Canonical Allele Identifier: PA2826220229
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 1422853
ClinVar RCV Id: RCV001945717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184147.1:p.Arg144Trp
CA3276398
NM_001197218.2:c.430C>T