Canonical Allele Identifier: PA327265
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53796
ClinVar RCV Id: RCV001387159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly1244Arg
CA327264
NM_000492.4:c.3730G>A
CA368974453
NM_000492.4:c.3730G>C