Canonical Allele Identifier: PA2826619639
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 195780
ClinVar RCV Id: RCV000194823 RCV000724440 RCV001086963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267470.1:p.Tyr909Asp
CA209252
NM_001280541.2:c.2725T>G