Canonical Allele Identifier: PA658703523
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 495902
ClinVar RCV Id: RCV000586088 RCV001834840 RCV001860127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ala534Ser
CA368975883
NM_000492.4:c.1600G>T