Canonical Allele Identifier: PA1139682590
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 917606
ClinVar RCV Id: RCV001174678 RCV003473719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ser1045Tyr
CA368990854
NM_000492.4:c.3134C>A