Canonical Allele Identifier: PA1139683820
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 853528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Phe1413Leu
CA4451666
NM_000492.4:c.4237T>C
CA368983831
NM_000492.4:c.4239T>A
CA368983832
NM_000492.4:c.4239T>G