Canonical Allele Identifier: PA2741880662
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 2996925
ClinVar RCV Id: RCV003859060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366538.1:p.Gln341Arg
CA9213108
NM_001379609.1:c.1022A>G