Canonical Allele Identifier: PA2580119623
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1796717
ClinVar RCV Id: RCV002435248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile947Thr
CA4451297
NM_000492.4:c.2840T>C