Canonical Allele Identifier: PA094652
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 35872
ClinVar RCV Id: RCV000029527 RCV000079000 RCV000755234 RCV001642238 RCV001163789 RCV001801912 RCV003333727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ser1235Arg
CA090908
NM_000492.4:c.3705T>G
CA368997556
NM_000492.4:c.3703A>C
CA368997568
NM_000492.4:c.3705T>A