Canonical Allele Identifier: PA326889
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53543
ClinVar RCV Id: RCV000667642 RCV001265632 RCV000508371 RCV001158765 RCV001284478 RCV002257389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ser895Asn
CA326888
NM_000492.4:c.2684G>A