Canonical Allele Identifier: PA147589
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 94079
ClinVar RCV Id: RCV000080027 RCV000381668 RCV001537232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002734.2:p.Ala291Thr
CA147588
NM_002743.3:c.871G>A