Canonical Allele Identifier: PA2580116028
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1693959
ClinVar RCV Id: RCV002261828 RCV002434612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr94Ile
CA4450700
NM_000492.4:c.281C>T