Canonical Allele Identifier: PA2825216013
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1964761
ClinVar RCV Id: RCV002726304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001329.1:p.Pro306Leu
CA9213066
NM_001001329.3:c.917C>T