Canonical Allele Identifier: PA2825192996
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 3233533
ClinVar RCV Id: RCV004526383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Met348Val
CA368978872
NM_000492.4:c.1042A>G