Canonical Allele Identifier: PA658669568
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 476044
ClinVar RCV Id: RCV000624406 RCV000542399 RCV001573188 RCV001336304 RCV004553245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.Ser924Ala
CA1580198
NM_015662.3:c.2770T>G