Canonical Allele Identifier: PA2826883647
Gene: IFT52 HGNC NCBI

Linked Data

ClinVar Variation Id: 253307
ClinVar RCV Id: RCV000240373 RCV000755169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290387.1:p.Ala199Thr
CA10586310
NM_001303458.2:c.595G>A