Allele Registry

Canonical Allele Identifier: PA1139681637

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV001228121

ClinVar Variation:

955475

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Ala559Ser	CA368976209 NM_000492.4:c.1675G>T