Canonical Allele Identifier: PA2826759689
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1964761
ClinVar RCV Id: RCV002726304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276033.1:p.Pro306Leu
CA9213066
NM_001289104.2:c.917C>T