Canonical Allele Identifier: PA916051250
Gene: PDE11A HGNC NCBI

Linked Data

ClinVar Variation Id: 713888
ClinVar RCV Id: RCV000886105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058649.3:p.Arg202Cys
CA1982227
NM_016953.3:c.604C>T