Allele Registry

Canonical Allele Identifier: PA2825194569

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV004518586

ClinVar Variation:

3231871

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Leu957Phe	CA368987416 NM_000492.4:c.2869C>T