Canonical Allele Identifier: PA2828842663
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 2332372
ClinVar RCV Id: RCV002925334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366537.1:p.Asp334Tyr
CA9213101
NM_001379608.1:c.1000G>T