Canonical Allele Identifier: PA158345
Gene: ECT2L HGNC NCBI

Linked Data

ClinVar Variation Id: 133988
ClinVar RCV Id: RCV000120657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001071174.1:p.Ile504Val
CA158344
NM_001077706.3:c.1510A>G