Canonical Allele Identifier: PA2828842634
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 2159185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366537.1:p.Thr312Arg
CA9213076
NM_001379608.1:c.935C>G