Canonical Allele Identifier: PA2825216038
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 2165596
ClinVar RCV Id: RCV003084451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001329.1:p.Glu317_Glu333dup
CA993549749
NM_001001329.3:c.951_1001dup