Canonical Allele Identifier: PA327220
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53763
ClinVar RCV Id: RCV000592921 RCV003235018 RCV002453356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asp1168Gly
CA327219
NM_000492.4:c.3503A>G