Canonical Allele Identifier: PA2826759276
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1973183
ClinVar RCV Id: RCV002731087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276031.1:p.Leu289Phe
CA9213052
NM_001289102.2:c.865C>T