Canonical Allele Identifier: PA2580119266
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1794943
ClinVar RCV Id: RCV002437403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asn901Ile
CA368986467
NM_000492.4:c.2702A>T