Canonical Allele Identifier: PA327133
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53709
ClinVar RCV Id: RCV000576929 RCV002281550
ClinVar Variation Id: 618905
ClinVar RCV Id: RCV000757800 RCV001004306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Trp1098Cys
CA327132
NM_000492.4:c.3294G>C
CA368992416
NM_000492.4:c.3294G>T