Canonical Allele Identifier: PA645510246
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 439083
ClinVar RCV Id: RCV000506108 RCV002329206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu1388Val
CA368983435
NM_000492.4:c.4162C>G