Canonical Allele Identifier: PA1139683481
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 848224
ClinVar RCV Id: RCV001051933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg1325Ser
CA368981783
NM_000492.4:c.3975A>C
CA368981799
NM_000492.4:c.3975A>T