Canonical Allele Identifier: PA2741814686
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2630690
ClinVar RCV Id: RCV004527914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asp651His
CA368978971
NM_000492.4:c.1951G>C