Canonical Allele Identifier: PA326584
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53322
ClinVar RCV Id: RCV000577731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg553Gly
CA326583
NM_000492.4:c.1657C>G