Canonical Allele Identifier: PA2827916079
Gene: PRKCD HGNC NCBI
ClinVar RCV:
RCV001878535
ClinVar Variation:
1358064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341608.1:p.Asp126Tyr
CA353233856
NM_001354679.2:c.376G>T