Canonical Allele Identifier: PA2580117875
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1778293
ClinVar RCV Id: RCV002414679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asp567Asn
CA368977082
NM_000492.4:c.1699G>A