Canonical Allele Identifier: PA2826955351
Gene: PRKCG HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303258.1:p.Asp480Tyr
CA259672
NM_001316329.2:c.1438G>T