Canonical Allele Identifier: PA094722
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 7155
ClinVar RCV Id: RCV000007575 RCV000763571 RCV001004455 RCV001810836 RCV003473027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ser492Phe
CA325551
NM_000492.4:c.1475C>T