Canonical Allele Identifier: PA356068
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 219537
ClinVar RCV Id: RCV000587447 RCV001160121 RCV001327945 RCV001762431 RCV000206091 RCV000664323 RCV003468932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu967Ser
CA350158
NM_000492.4:c.2900T>C