Canonical Allele Identifier: PA2828842617
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 890258
ClinVar RCV Id: RCV001124703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366537.1:p.Glu283Lys
CA9213020
NM_001379608.1:c.847G>A