Canonical Allele Identifier: PA199771
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 191366
ClinVar RCV Id: RCV002508142 RCV003765075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.His1567Gln
CA199770
NM_015662.3:c.4701C>A
CA346415456
NM_015662.3:c.4701C>G