ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828842953
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_001366538.1:p.Thr312Arg
CA9213076
NM_001379609.1:c.935C>G