Canonical Allele Identifier: PA094524
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53733

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Met1137Val
CA327169
NM_000492.4:c.3409A>G