Allele Registry

Canonical Allele Identifier: PA2573170898

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV001990857

ClinVar Variation:

1479079

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.His954Tyr	CA4451302 NM_000492.4:c.2860C>T