Canonical Allele Identifier: PA2825216071
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 328188
ClinVar RCV Id: RCV000282905 RCV000885100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001329.1:p.Ala326Thr
CA9213094
NM_001001329.3:c.976G>A