Canonical Allele Identifier: PA2580120470
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1730761
ClinVar RCV Id: RCV002451770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly1125Glu
CA368993278
NM_000492.4:c.3374G>A