Canonical Allele Identifier: PA094122
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 54088
ClinVar RCV Id: RCV000576978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly314Arg
CA327695
NM_000492.4:c.940G>C
CA368978359
NM_000492.4:c.940G>A