Canonical Allele Identifier: PA2580120815
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1706020
ClinVar RCV Id: RCV002284550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asp1270Val
CA368975100
NM_000492.4:c.3809A>T