Canonical Allele Identifier: PA891863704
Gene: IFT140 HGNC NCBI

Linked Data

ClinVar Variation Id: 591375
ClinVar RCV Id: RCV000722554 RCV001862121
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055529.2:p.Gln1138Leu
CA7813181
NM_014714.4:c.3413A>T
CA891863054
NM_014714.4:c.3413_3414delinsTA