Canonical Allele Identifier: PA2826759511
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 2996925
ClinVar RCV Id: RCV003859060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276032.1:p.Gln341Arg
CA9213108
NM_001289103.2:c.1022A>G