Canonical Allele Identifier: PA1139700447
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 713728
ClinVar RCV Id: RCV000885917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002734.2:p.Glu323_Glu325del
CA9213080
NM_002743.3:c.960_968del
CA2582534205
NM_002743.3:c.963_971del