Canonical Allele Identifier: PA2580119052
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2453625
ClinVar RCV Id: RCV003187760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr816Pro
CA368981359
NM_000492.4:c.2446A>C