Canonical Allele Identifier: PA2741815160
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2567870
ClinVar RCV Id: RCV003283383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.His1402Arg
CA368983679
NM_000492.4:c.4205A>G