Canonical Allele Identifier: PA913194037
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 597314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly126Val
CA368974528
NM_000492.4:c.377G>T