Canonical Allele Identifier: PA1139681022
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 863689
ClinVar RCV Id: RCV001070714 RCV001283963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly437Asp
CA4450971
NM_000492.4:c.1310G>A