Canonical Allele Identifier: PA2829401413
Gene: PPP1CB HGNC NCBI

Linked Data

ClinVar Variation Id: 1488554
ClinVar RCV Id: RCV001988643

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002700.1:p.Ser47Arg
CA346581050
NM_002709.3:c.139A>C
CA346581065
NM_002709.3:c.141C>A
CA346581066
NM_002709.3:c.141C>G