Canonical Allele Identifier: PA2828842610
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 3025677
ClinVar RCV Id: RCV003885065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366537.1:p.Ala274_Arg277del
CA632117043
NM_001379608.1:c.821_832del