Canonical Allele Identifier: PA279863
Gene: PPP1R13B HGNC NCBI

Linked Data

ClinVar Variation Id: 208406
ClinVar RCV Id: RCV000202339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056131.2:p.Arg72Gln
CA279862
NM_015316.3:c.215G>A