Canonical Allele Identifier: PA327006
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53622
ClinVar RCV Id: RCV000046751 RCV001826652 RCV002262607 RCV003476944 RCV002477157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Met1Thr