Canonical Allele Identifier: PA2825193837
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 3231841
ClinVar RCV Id: RCV004518556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gln652Glu
CA4451123
NM_000492.4:c.1954C>G