Canonical Allele Identifier: PA2580119352
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2453638
ClinVar RCV Id: RCV003187773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Met929Ile
CA368986843
NM_000492.4:c.2787G>A
CA368986845
NM_000492.4:c.2787G>C
CA368986847
NM_000492.4:c.2787G>T