Canonical Allele Identifier: PA158386
Gene: ECT2L HGNC NCBI

Linked Data

ClinVar Variation Id: 134002
ClinVar RCV Id: RCV000120671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001181966.1:p.Arg827Trp
CA158384
NM_001195037.2:c.2479C>T