Canonical Allele Identifier: PA2826759271
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1255532
ClinVar RCV Id: RCV001844861 RCV002539633 RCV002488450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276031.1:p.Arg281Trp
CA9213015
NM_001289102.2:c.841C>T