Canonical Allele Identifier: PA2580117376
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1775173
ClinVar RCV Id: RCV002405326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ser519Arg
CA368984894
NM_000492.4:c.1555A>C
CA368984901
NM_000492.4:c.1557C>A
CA368984903
NM_000492.4:c.1557C>G