Canonical Allele Identifier: PA327671
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 54071
ClinVar RCV Id: RCV000594718 RCV000577467 RCV002483059 RCV002469001 RCV001831805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asn287Lys
CA327670
NM_000492.4:c.861C>G
CA368977574
NM_000492.4:c.861C>A