Canonical Allele Identifier: PA2826759497
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 2000522
ClinVar RCV Id: RCV002824592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276032.1:p.Glu320_Glu333del
CA2580096631
NM_001289103.2:c.960_1001del