Canonical Allele Identifier: PA2826759277
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 94079
ClinVar RCV Id: RCV000080027 RCV000381668 RCV001537232
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276031.1:p.Ala291Thr
CA147588
NM_001289102.2:c.871G>A