Canonical Allele Identifier: PA2825215996
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 94079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001329.1:p.Ala291Thr
CA147588
NM_001001329.3:c.871G>A