Canonical Allele Identifier: PA2580116721
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1732049
ClinVar RCV Id: RCV002337533 RCV003475341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr382Pro
CA4450910
NM_000492.4:c.1144A>C