Allele Registry

Canonical Allele Identifier: PA2499232878

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV001420891

ClinVar Variation:

1098811

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Leu165Phe	CA368976322 NM_000492.4:c.495A>C CA368976324 NM_000492.4:c.495A>T