Canonical Allele Identifier: PA2825216104
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 2996925
ClinVar RCV Id: RCV003859060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001329.1:p.Gln341Arg
CA9213108
NM_001001329.3:c.1022A>G