Canonical Allele Identifier: PA2580119250
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2453630
ClinVar RCV Id: RCV003187765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly893Arg
CA368986408
NM_000492.4:c.2677G>A
CA368986409
NM_000492.4:c.2677G>C