Canonical Allele Identifier: PA326705
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 35833
ClinVar RCV Id: RCV000046498 RCV000506455 RCV001009381 RCV001004277 RCV000763577 RCV001588828 RCV002228058 RCV002256004 RCV003473129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly622Asp
CA326704
NM_000492.4:c.1865G>A