Canonical Allele Identifier: PA2580120819
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1735164
ClinVar RCV Id: RCV002355253 RCV003146542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly1271Ser
CA368975114
NM_000492.4:c.3811G>A