Canonical Allele Identifier: PA2827915800
Gene: PRKCD HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341607.1:p.Ala228Val
CA2451901
NM_001354678.2:c.683C>T