Canonical Allele Identifier: PA094090
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 35881
ClinVar RCV Id: RCV000029536 RCV000211255 RCV001826515 RCV002247398 RCV002477013 RCV003473145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly1349Asp
CA325711
NM_000492.4:c.4046G>A