Canonical Allele Identifier: PA2580121645
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2447409
ClinVar RCV Id: RCV003165234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr1380Ile
CA368983314
NM_000492.4:c.4139C>T