Canonical Allele Identifier: PA2741818514
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2567857
ClinVar RCV Id: RCV003311474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ala209Val
CA368976870
NM_000492.4:c.626C>T