Canonical Allele Identifier: PA2827195354
Gene: IFT52 HGNC NCBI

Linked Data

ClinVar Variation Id: 253307
ClinVar RCV Id: RCV000240373 RCV000755169
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310507.1:p.Ala23Thr
CA10586310
NM_001323578.2:c.67G>A