Canonical Allele Identifier: PA2829401431
Gene: PPP1CB HGNC NCBI

Linked Data

ClinVar Variation Id: 427633
ClinVar RCV Id: RCV000490624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002700.1:p.Ala56Pro
CA346581171
NM_002709.3:c.166G>C