Canonical Allele Identifier: PA2826620285
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 530928
ClinVar RCV Id: RCV000637014 RCV001756057 RCV004025487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001267475.1:p.Asp209Asn
CA2606114
NM_001280546.2:c.625G>A