Canonical Allele Identifier: PA2573170848
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1468980
ClinVar RCV Id: RCV001972908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ala763Thr
CA368980850
NM_000492.4:c.2287G>A