Canonical Allele Identifier: PA260257
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 35887
ClinVar RCV Id: RCV000029542 RCV003234922 RCV000593356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ala198Thr
CA260256
NM_000492.4:c.592G>A