Canonical Allele Identifier: PA658803799
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 526015
ClinVar RCV Id: RCV000630453 RCV000781232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile448Thr
CA368982204
NM_000492.4:c.1343T>C