Allele Registry

Canonical Allele Identifier: PA326616

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000577294

RCV001269511

ClinVar Variation:

53346

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Trp57Arg	CA326615 NM_000492.4:c.169T>C CA368972112 NM_000492.4:c.169T>A