Canonical Allele Identifier: PA093924
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53358
ClinVar RCV Id: RCV000577056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asp572Asn
CA326631
NM_000492.4:c.1714G>A