Canonical Allele Identifier: PA658803857
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 497599
ClinVar RCV Id: RCV000594547 RCV001245034 RCV002491175 RCV001834866 RCV003994036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly1173Ser
CA4451489
NM_000492.4:c.3517G>A