Canonical Allele Identifier: PA2830523115
Gene: PRKCD HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997704.1:p.Asp126Tyr
CA353233856
NM_212539.2:c.376G>T