Canonical Allele Identifier: PA2827736886
Gene: CELF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 493234
ClinVar RCV Id: RCV000585277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340679.1:p.Ser25Asn
CA402040769
NM_001353750.2:c.74G>A