Canonical Allele Identifier: PA326897
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53547
ClinVar RCV Id: RCV000668207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile907Val
CA326896
NM_000492.4:c.2719A>G