Canonical Allele Identifier: PA916039073
Gene: PRKCD HGNC NCBI

Linked Data

ClinVar Variation Id: 440191
ClinVar RCV Id: RCV000506287 RCV001081059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341605.1:p.Asn367Ser
CA2452073
NM_001354676.2:c.1100A>G