Canonical Allele Identifier: PA2826759700
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 94081
ClinVar RCV Id: RCV000080029 RCV000377384 RCV001636642
ClinVar Variation Id: 2027674
ClinVar RCV Id: RCV002866736
ClinVar Variation Id: 2722881
ClinVar RCV Id: RCV003559128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276033.1:p.Glu325del
CA147592
NM_001289104.2:c.966_968del
CA9213087
NM_001289104.2:c.972_974del