Canonical Allele Identifier: PA2573170857
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1429215
ClinVar RCV Id: RCV001938817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Glu827del
CA2580614250
NM_000492.4:c.2481_2483del