Canonical Allele Identifier: PA2580115994
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1730745
ClinVar RCV Id: RCV002451754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Tyr38Cys
CA4450639
NM_000492.4:c.113A>G