Canonical Allele Identifier: PA326899
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53548
ClinVar RCV Id: RCV000577705 RCV001009494 RCV003235015 RCV003473492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr908Asn
CA326898
NM_000492.4:c.2723C>A