Canonical Allele Identifier: PA327098
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53684
ClinVar RCV Id: RCV000046823 RCV000506564 RCV001009473 RCV002226453 RCV003474569 RCV001375487
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly1069Arg
CA327097
NM_000492.4:c.3205G>A
CA368992085
NM_000492.4:c.3205G>C