Canonical Allele Identifier: PA2741814896
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2637539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asp993Gly
CA4451342
NM_000492.4:c.2978A>G