Canonical Allele Identifier: PA2828842650
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1352743
ClinVar RCV Id: RCV002039921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366537.1:p.Glu323_Glu325dup
CA305355918
NM_001379608.1:c.960_968dup
CA2582534210
NM_001379608.1:c.968_969insGGAAGAGGA