Canonical Allele Identifier: PA2825578794
Gene: PABPC4L HGNC NCBI

Linked Data

ClinVar Variation Id: 2330161
ClinVar RCV Id: RCV004176658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108206.3:p.Gly231Cys
CA3081043
NM_001114734.2:c.691G>T