Canonical Allele Identifier: PA094382
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 7208
ClinVar RCV Id: RCV000007629 RCV000311326 RCV001004297 RCV001831550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu1065Pro
CA325596
NM_000492.4:c.3194T>C