Canonical Allele Identifier: PA2573062905
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1313092
ClinVar RCV Id: RCV001769043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg1162Pro
CA164976465
NM_000492.4:c.3485G>C