Canonical Allele Identifier: PA1139683301
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 971487
ClinVar RCV Id: RCV001247277 RCV001830007 RCV003331090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg1283Ser
CA368975486
NM_000492.4:c.3849G>C
CA368975489
NM_000492.4:c.3849G>T