Canonical Allele Identifier: PA2828842619
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 890827
ClinVar RCV Id: RCV001125709 RCV001856648 RCV003293892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366537.1:p.Asp288Asn
CA9213051
NM_001379608.1:c.862G>A