Canonical Allele Identifier: PA658675657
Gene: IFT74 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079379.2:p.Gly352Cys
CA5015490
NM_025103.2:c.1054G>T