Canonical Allele Identifier: PA913194326
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 633158
ClinVar RCV Id: RCV000781241 RCV002360901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Pro1290Thr
CA4451560
NM_000492.4:c.3868C>A