Allele Registry

Canonical Allele Identifier: PA326463

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000046286

ClinVar Variation:

53238

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Ala46Asp	CA326462 NM_000492.4:c.137C>A