Canonical Allele Identifier: PA2573171092
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1402955
ClinVar RCV Id: RCV001897086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu1388Pro
CA368983443
NM_000492.4:c.4163T>C