Canonical Allele Identifier: PA2825194839
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 3143846
ClinVar RCV Id: RCV004436652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg1158Leu
CA368995932
NM_000492.4:c.3473G>T