Canonical Allele Identifier: PA658681935
Gene: IFT80 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065851.1:p.Ile191Asn
CA2685433
NM_020800.3:c.572T>A