Canonical Allele Identifier: PA2825215975
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 1255532
ClinVar RCV Id: RCV001844861 RCV002539633 RCV002488450
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001329.1:p.Arg281Trp
CA9213015
NM_001001329.3:c.841C>T