Canonical Allele Identifier: PA2826955008
Gene: PRKCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2197891
ClinVar RCV Id: RCV002640277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303256.1:p.Lys260Gln
CA74812640
NM_001316327.2:c.778A>C