Canonical Allele Identifier: PA2828842625
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 94079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366537.1:p.Ala291Thr
CA147588
NM_001379608.1:c.871G>A