Canonical Allele Identifier: PA2580121696
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1706050
ClinVar RCV Id: RCV002284580 RCV003478958 RCV004526923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Met1407Thr
CA368983750
NM_000492.4:c.4220T>C