Canonical Allele Identifier: PA2580117889
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2064880
ClinVar RCV Id: RCV002928921 RCV003317632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ser573Cys
CA368977184
NM_000492.4:c.1718C>G