Canonical Allele Identifier: PA2580119239
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1717676
ClinVar RCV Id: RCV002297701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Val879Asp
CA368985991
NM_000492.4:c.2636T>A