Canonical Allele Identifier: PA2741814535
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2769610
ClinVar RCV Id: RCV003507900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asp443Val
CA368982045
NM_000492.4:c.1328A>T