Canonical Allele Identifier: PA916039080
Gene: PRKCD HGNC NCBI

Linked Data

ClinVar Variation Id: 252661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341605.1:p.Arg502Gln
CA10585980
NM_001354676.2:c.1505G>A