Canonical Allele Identifier: PA2826759698
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 94080
ClinVar RCV Id: RCV000080028 RCV001668195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276033.1:p.Glu324_Glu325del
CA147590
NM_001289104.2:c.963_968del
CA9213086
NM_001289104.2:c.966_971del