Canonical Allele Identifier: PA2827915945
Gene: PRKCD HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341607.1:p.Gly526Ser
CA171032
NM_001354678.2:c.1576G>A