Canonical Allele Identifier: PA326382
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53176
ClinVar RCV Id: RCV000577480 RCV001731337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gln353His
CA326381
NM_000492.4:c.1059A>C
CA368978923
NM_000492.4:c.1059A>T