Allele Registry

Canonical Allele Identifier: PA326495

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV001009387

ClinVar Variation:

53261

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Cys491Arg	CA326494 NM_000492.4:c.1471T>C