Canonical Allele Identifier: PA1139700403
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 890258
ClinVar RCV Id: RCV001124703

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002734.2:p.Glu283Lys
CA9213020
NM_002743.3:c.847G>A