Allele Registry

Canonical Allele Identifier: PA326992

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000577122

RCV001009535

ClinVar Variation:

53610

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Pro99Leu	CA326991 NM_000492.4:c.296C>T