Canonical Allele Identifier: PA913194128
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 595238
ClinVar RCV Id: RCV000730739 RCV000781287 RCV001324938 RCV001830608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Lys536Glu
CA4451044
NM_000492.4:c.1606A>G