Canonical Allele Identifier: PA2825216027
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 2059757
ClinVar RCV Id: RCV002957251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001329.1:p.Glu324_Glu325dup
CA305355924
NM_001001329.3:c.963_968dup
CA632117108
NM_001001329.3:c.966_971dup