Canonical Allele Identifier: PA2580147731
Gene: PRCD HGNC NCBI

Linked Data

ClinVar Variation Id: 1929516
ClinVar RCV Id: RCV002635404 RCV003324584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001071088.1:p.Ser38Ter
CA986412903
NM_001077620.3:c.102_111dup