Canonical Allele Identifier: PA2826759282
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 2262690
ClinVar RCV Id: RCV002778521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276031.1:p.Ser310Leu
CA9213073
NM_001289102.2:c.929C>T