Canonical Allele Identifier: PA658827187
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 554293
ClinVar RCV Id: RCV000669903 RCV001174826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu102Arg
CA4450702
NM_000492.4:c.305T>G