Canonical Allele Identifier: PA158385
Gene: ECT2L HGNC NCBI

Linked Data

ClinVar Variation Id: 134002
ClinVar RCV Id: RCV000120671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001071174.1:p.Arg827Trp
CA158384
NM_001077706.3:c.2479C>T