Allele Registry

Canonical Allele Identifier: PA327358

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000672177

RCV003478988

ClinVar Variation:

53858

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Gln1313Lys	CA327357 NM_000492.4:c.3937C>A