Canonical Allele Identifier: PA2580120535
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2443365
ClinVar RCV Id: RCV003151972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Trp1145Ser
CA368993597
NM_000492.4:c.3434G>C