Canonical Allele Identifier: PA2499232884
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1038737

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile482Val
CA368984434
NM_000492.4:c.1444A>G