Canonical Allele Identifier: PA658754747
Gene: CWF19L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 488455
ClinVar RCV Id: RCV001093418 RCV000578265
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060764.3:p.Glu519del
CA5646826
NM_018294.6:c.1555_1557del