Canonical Allele Identifier: PA2826759711
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 193858
ClinVar RCV Id: RCV000174068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276033.1:p.Glu333dup
CA239536
NM_001289104.2:c.999_1001dup