Canonical Allele Identifier: PA2825193652
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 3231833
ClinVar RCV Id: RCV004518548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile586Thr
CA368977289
NM_000492.4:c.1757T>C