Canonical Allele Identifier: PA094101
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53951
ClinVar RCV Id: RCV000577096 RCV003883127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly149Arg
CA327493
NM_000492.4:c.445G>A
CA368974913
NM_000492.4:c.445G>C