Canonical Allele Identifier: PA2580439161
Gene: IFT46 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064538.3:p.Asn341Ser
CA6305604
NM_020153.4:c.1022A>G