Canonical Allele Identifier: PA2826759716
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 2057120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276033.1:p.Val337Met
CA9213105
NM_001289104.2:c.1009G>A