Canonical Allele Identifier: PA2826759502
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 328188
ClinVar RCV Id: RCV000282905 RCV000885100
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276032.1:p.Ala326Thr
CA9213094
NM_001289103.2:c.976G>A