Canonical Allele Identifier: PA2580120740
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1734301
ClinVar RCV Id: RCV002349102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly1241Ser
CA368974409
NM_000492.4:c.3721G>A