Canonical Allele Identifier: PA658827207
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 554722
ClinVar RCV Id: RCV000670402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Trp356Ser
CA4450885
NM_000492.4:c.1067G>C