Canonical Allele Identifier: PA327478
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53940
ClinVar RCV Id: RCV000577681 RCV001731341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg1438Trp
CA327477
NM_000492.4:c.4312C>T