Canonical Allele Identifier: PA2826156821
Gene: IFT80 HGNC NCBI
ClinVar RCV:
RCV000515810
ClinVar Variation:
446653
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177171.1:p.Leu384Phe
CA355191342
NM_001190242.2:c.1150C>T