Canonical Allele Identifier: PA093780
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 7198
ClinVar RCV Id: RCV000007619 RCV000660773 RCV000763568 RCV000985669 RCV001004254 RCV001826444 RCV003473041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg352Gln
CA325583
NM_000492.4:c.1055G>A