Canonical Allele Identifier: PA152328
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 35839
ClinVar RCV Id: RCV000029494 RCV000116686 RCV000119039 RCV000513754 RCV000582582 RCV001095213 RCV001249413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg75Gln
CA152327
NM_000492.4:c.224G>A