Canonical Allele Identifier: PA2741814516
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2567888
ClinVar RCV Id: RCV003283393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr398Lys
CA368980217
NM_000492.4:c.1193C>A