Canonical Allele Identifier: PA171033
Gene: PRKCD HGNC NCBI
ClinVar RCV:
RCV000144965
ClinVar Variation:
157674
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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