Canonical Allele Identifier: PA325717
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 35893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg31Cys
CA325716
NM_000492.4:c.91C>T