Canonical Allele Identifier: PA2580120084
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2496643
ClinVar RCV Id: RCV003221246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gln1042Arg
CA368990836
NM_000492.4:c.3125A>G