Canonical Allele Identifier: PA2741815101
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2637481
ClinVar RCV Id: RCV003404779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu1324Phe
CA368981756
NM_000492.4:c.3970C>T