Canonical Allele Identifier: PA2741814850
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2624954
ClinVar RCV Id: RCV003377633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Pro936Ser
CA368986956
NM_000492.4:c.2806C>T