Canonical Allele Identifier: PA2827916523
Gene: PRKCD HGNC NCBI

Linked Data

ClinVar Variation Id: 440191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341609.1:p.Asn348Ser
CA2452073
NM_001354680.2:c.1043A>G