Canonical Allele Identifier: PA2825216077
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1255647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001329.1:p.Glu330Lys
CA404136060
NM_001001329.3:c.988G>A