Canonical Allele Identifier: PA2573170418
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1415535
ClinVar RCV Id: RCV001921011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile105Leu
CA368974329
NM_000492.4:c.313A>C