Canonical Allele Identifier: PA645403577
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 411126
ClinVar RCV Id: RCV000457331 RCV001833593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asn396Tyr
CA4450917
NM_000492.4:c.1186A>T