Canonical Allele Identifier: PA199774
Gene: IFT172 HGNC NCBI

Linked Data

ClinVar Variation Id: 191368
ClinVar RCV Id: RCV000171550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056477.1:p.Asp1605Glu
CA199773
NM_015662.3:c.4815T>G
CA346414999
NM_015662.3:c.4815T>A