Canonical Allele Identifier: PA2580116064
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1740622
ClinVar RCV Id: RCV002328273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile148Ser
CA368974902
NM_000492.4:c.443T>G