Canonical Allele Identifier: PA2573170388
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1379486
ClinVar RCV Id: RCV001883796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ala62Ser
CA368972138
NM_000492.4:c.184G>T