This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA916066737
Gene: PPP1R1B HGNC NCBI
ClinVar RCV:
RCV000955271
ClinVar Variation:
775160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115568.2:p.Ser198Tyr
CA8532144
NM_032192.4:c.593C>A