Canonical Allele Identifier: PA645403379
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 281724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Phe316Leu
CA10603955
NM_000492.4:c.948T>G
CA368978420
NM_000492.4:c.946T>C
CA368978427
NM_000492.4:c.948T>A