Allele Registry

Canonical Allele Identifier: PA913194135

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000757828

ClinVar Variation:

618927

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Tyr563His	CA368977018 NM_000492.4:c.1687T>C