Canonical Allele Identifier: PA2580119251
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1794686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asn894Ser
CA368986417
NM_000492.4:c.2681A>G