Canonical Allele Identifier: PA2499232882
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1055358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly314Ala
CA368978366
NM_000492.4:c.941G>C