Canonical Allele Identifier: PA2580118080
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1784814
ClinVar RCV Id: RCV002419843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Trp679Arg
CA368979333
NM_000492.4:c.2035T>A
CA368979334
NM_000492.4:c.2035T>C