Canonical Allele Identifier: PA2573170381
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1408121
ClinVar RCV Id: RCV001909808 RCV002469429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asn48His
CA368987414
NM_000492.4:c.142A>C