Canonical Allele Identifier: PA2825216018
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 2159185
ClinVar RCV Id: RCV003072685 RCV003072684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001329.1:p.Thr312Arg
CA9213076
NM_001001329.3:c.935C>G