Canonical Allele Identifier: PA2573170374
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1493230
ClinVar RCV Id: RCV001984216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ser35Leu
CA368987151
NM_000492.4:c.104C>T