Canonical Allele Identifier: PA1139680276
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 973864
ClinVar RCV Id: RCV001250527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu69Ile
CA164936980
NM_000492.4:c.205C>A