Canonical Allele Identifier: PA093863
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 7136
ClinVar RCV Id: RCV000007556 RCV000224445 RCV001004513 RCV001831530 RCV002255995 RCV002287325 RCV003473015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asn1303Lys
CA340641
NM_000492.4:c.3909C>G
CA368978243
NM_000492.4:c.3909C>A