Canonical Allele Identifier: PA2741818500
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2581464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Tyr84Cys
CA4450674
NM_000492.4:c.251A>G