Canonical Allele Identifier: PA2573205363
Gene: PRKCD HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341605.1:p.Asp145Tyr
CA353233856
NM_001354676.2:c.433G>T