Canonical Allele Identifier: PA2580119033
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1790972
ClinVar RCV Id: RCV002459769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asp806Glu
CA368981198
NM_000492.4:c.2418T>A
CA368981200
NM_000492.4:c.2418T>G