Canonical Allele Identifier: PA2741814609
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2562518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly542Glu
CA4451047
NM_000492.4:c.1625G>A