Canonical Allele Identifier: PA2826759281
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1964761
ClinVar RCV Id: RCV002726304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276031.1:p.Pro306Leu
CA9213066
NM_001289102.2:c.917C>T