Canonical Allele Identifier: PA327664
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 54065
ClinVar RCV Id: RCV000577038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Trp277Arg
CA327663
NM_000492.4:c.829T>A
CA368977500
NM_000492.4:c.829T>C