Canonical Allele Identifier: PA2825216010
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 328186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001329.1:p.Pro305Leu
CA9213063
NM_001001329.3:c.914C>T