Canonical Allele Identifier: PA171033
Gene: PRKCD HGNC NCBI

Linked Data

ClinVar Variation Id: 157674
ClinVar RCV Id: RCV000144965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006245.2:p.Gly510Ser
CA171032
NM_006254.4:c.1528G>A