Canonical Allele Identifier: PA916039083
Gene: PRKCD HGNC NCBI

Linked Data

ClinVar Variation Id: 157674
ClinVar RCV Id: RCV000144965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341605.1:p.Gly529Ser
CA171032
NM_001354676.2:c.1585G>A