Canonical Allele Identifier: PA2580120486
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1731074
ClinVar RCV Id: RCV002452083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr1134Asn
CA368993413
NM_000492.4:c.3401C>A