Canonical Allele Identifier: PA915957182
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 821923
ClinVar RCV Id: RCV002319622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ser955Ala
CA368987390
NM_000492.4:c.2863T>G