Canonical Allele Identifier: PA2825216085
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 2057120
ClinVar RCV Id: RCV002914783 RCV004067120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001329.1:p.Val337Met
CA9213105
NM_001001329.3:c.1009G>A