Canonical Allele Identifier: PA095614
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 31683
ClinVar RCV Id: RCV000024363 RCV000255441 RCV000515934 RCV001328311 RCV000626465 RCV001249674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Gly212Arg
CA129889
NM_014714.4:c.634G>A
CA394220095
NM_014714.4:c.634G>C