Canonical Allele Identifier: PA2826882133
Gene: CWF19L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 488455
ClinVar RCV Id: RCV001093418 RCV000578265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290333.1:p.Glu479del
CA5646826
NM_001303404.2:c.1435_1437del