Canonical Allele Identifier: PA2499232878
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1098811
ClinVar RCV Id: RCV001420891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu165Phe
CA368976322
NM_000492.4:c.495A>C
CA368976324
NM_000492.4:c.495A>T