Canonical Allele Identifier: PA2580116826
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1770553
ClinVar RCV Id: RCV002387901 RCV003738238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg450Ile
CA368982249
NM_000492.4:c.1349G>T