Canonical Allele Identifier: PA327421
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53900
ClinVar RCV Id: RCV000577023 RCV003398629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Tyr1381His
CA327420
NM_000492.4:c.4141T>C