Canonical Allele Identifier: PA327179
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53738
ClinVar RCV Id: RCV000576944 RCV004018953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Met1140Lys
CA327178
NM_000492.4:c.3419T>A