Allele Registry

Canonical Allele Identifier: PA094870

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000577252

RCV000985680

ClinVar Variation:

53351

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Tyr569His	CA326623 NM_000492.4:c.1705T>C