Canonical Allele Identifier: PA645448779
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 373496
ClinVar RCV Id: RCV000413813 RCV001073846 RCV001248514 RCV002521422 RCV004551413 RCV002481279
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.Glu277Asp
CA1580852
NM_015662.3:c.831G>C
CA346397231
NM_015662.3:c.831G>T