Canonical Allele Identifier: PA2828098229
Gene: PABPC4L HGNC NCBI

Linked Data

ClinVar Variation Id: 3207846
ClinVar RCV Id: RCV004497688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350514.1:p.Ser236Thr
CA106325730
NM_001363585.1:c.707G>C