Canonical Allele Identifier: PA2741814939
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2808233
ClinVar RCV Id: RCV003618356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Phe1068Val
CA368992066
NM_000492.4:c.3202T>G