Canonical Allele Identifier: PA2828842629
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1964761
ClinVar RCV Id: RCV002726304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366537.1:p.Pro306Leu
CA9213066
NM_001379608.1:c.917C>T