Canonical Allele Identifier: PA913194038
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 595383
ClinVar RCV Id: RCV000730911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr135Ala
CA368974662
NM_000492.4:c.403A>G