Canonical Allele Identifier: PA1139682594
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 950097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly1047Ser
CA368990865
NM_000492.4:c.3139G>A