Canonical Allele Identifier: PA327593
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 54021
ClinVar RCV Id: RCV000507508 RCV001705707 RCV001009495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Phe200Ile
CA327592
NM_000492.4:c.598T>A