Canonical Allele Identifier: PA2825578784
Gene: PABPC4L HGNC NCBI

Linked Data

ClinVar Variation Id: 3207841
ClinVar RCV Id: RCV004497683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108206.3:p.Met84Thr
CA358375491
NM_001114734.2:c.251T>C