Canonical Allele Identifier: PA2825216049
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1909841
ClinVar RCV Id: RCV002600487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001329.1:p.Glu314Gly
CA404135944
NM_001001329.3:c.941A>G