Canonical Allele Identifier: PA326943
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53578
ClinVar RCV Id: RCV000577071 RCV001290523 RCV001835661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.His949Leu
CA326942
NM_000492.4:c.2846A>T