Canonical Allele Identifier: PA2741818508
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2567867
ClinVar RCV Id: RCV003311481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile160Thr
CA368975151
NM_000492.4:c.479T>C