Canonical Allele Identifier: PA2580119737
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1797761
ClinVar RCV Id: RCV002440011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Phe976Leu
CA4451330
NM_000492.4:c.2928C>G
CA4451331
NM_000492.4:c.2928C>A
CA368988986
NM_000492.4:c.2926T>C