Canonical Allele Identifier: PA2741814495
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2573422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ala357Val
CA368978964
NM_000492.4:c.1070C>T